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1. Is not a ‘‘significant regulatory the rudder brackets-hinge and bearings for Issued in Kansas City, Missouri, on
action’’ under Executive Order 12866; corrosion and lubricate the rudder bearings February 20, 2007.
2. Is not a ‘‘significant rule’’ under the in accordance with the accomplishment David R. Showers,
DOT Regulatory Policies and Procedures instructions of REIMS AVIATION Acting Manager, Small Airplane Directorate,
(44 FR 11034, February 26, 1979); and INDUSTRIES Service Bulletin No. F406–57, Aircraft Certification Service.
3. Will not have a significant dated April 25, 2005. If corrosion is found, [FR Doc. E7–3399 Filed 2–26–07; 8:45 am]
economic impact, positive or negative, replace these parts before further flight
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(2) Initially lubricate the rudder bearings
on a substantial number of small entities
within 600 hours time-in-service or within 12
under the criteria of the Regulatory months, whichever occurs first, after the
Flexibility Act. effective date of this AD, and repetitively DEPARTMENT OF TRANSPORTATION
We prepared a regulatory evaluation thereafter at intervals not to exceed 12
of the estimated costs to comply with Federal Aviation Administration
months. During this step, remove the rudder
this proposed AD and placed it in the to realize an optimum inspection and
AD docket. lubrication in accordance with the 14 CFR Part 145
accomplishment instructions of Reims [Docket No. FAA–2006–26408]
List of Subjects in 14 CFR Part 39
Aviation Industries Service Bulletin No.
Air transportation, Aircraft, Aviation F406–57, dated April 25, 2005. RIN 2120–AI53
safety, Safety. Note 1: We have established the repetitive
Repair Stations; Extension of
The Proposed Amendment inspection times of this AD so that they may
Comment Period
coincide with annual inspections.
Accordingly, under the authority AGENCY: Federal Aviation
Note 2: We encourage you to put Reims
delegated to me by the Administrator, Administration (FAA), DOT.
temporary revision No. 4 into the
the FAA proposes to amend 14 CFR part maintenance program of the F406 airplane ACTION: Notice of proposed rulemaking
39 as follows: (chapter 5–10–01, page 17 of the (NPRM); extension of comment period.
maintenance manual).
PART 39—AIRWORTHINESS SUMMARY: This action extends the
DIRECTIVES FAA AD Differences comment period for the Repair Stations
1. The authority citation for part 39 Note 3: This AD differs from the MCAI NPRM, Docket No. FAA–2006–26408
continues to read as follows: and/or service information as follows: We that was published on December 1,
have added repetitive inspection 2006. In that document, the FAA
Authority: 49 U.S.C. 106(g), 40113, 44701. requirements in the AD to coincide with the proposed to amend the regulations for
§ 39.13 [Amended] maintenance requirement in the service repair stations by revising the system of
bulletin. ratings and requiring repair stations to
2. The FAA amends § 39.13 by adding
establish a quality program. The FAA
the following new AD: Other FAA AD Provisions
also proposed additional changes
REIMS AVIATION S.A.: Docket No. FAA– (f) The following provisions also apply to critical to maintaining safety. On
2006–26692; Directorate Identifier 2006– this AD: January 26, 2007, the Aeronautical
CE–89–AD (1) Alternative Methods of Compliance Repair Station Association (ARSA)
(AMOCs): The Manager, Standards Staff,
Comments Due Date
FAA, ATTN: Mike Kiesov, Aerospace
requested an extension to the comment
(a) We must receive comments by March Engineer, FAA, Small Airplane Directorate, period for this NPRM. The FAA has
29, 2007. 901 Locust, Room 301, Kansas City, Missouri, considered this request and decided to
64106; telephone: (816) 329–4144; fax: (816) extend the comment period for 45 days.
Affected ADs
329–4090, has the authority to approve DATES: Comments must be received on
(b) None. AMOCs for this AD, if requested using the or before April 16, 2007.
Applicability procedures found in 14 CFR 39.19. ADDRESSES: You may send comments,
(c) This AD applies to Reims Aviation S.A. (2) Airworthy Product: For any identified by Docket Number FAA–
Model F406 airplanes, serial numbers F406– requirement in this AD to obtain corrective
2006–26408, using any of the following
0001 through F406–0092, certificated in any actions from a manufacturer or other source,
use these actions if they are FAA-approved.
methods:
category.
Corrective actions are considered FAA-
• DOT Docket Web site: Go to
Reason approved if they are approved by the State http://dms.dot.gov and follow the
(d) The mandatory continuing of Design Authority (or their delegated instructions for sending your comments
airworthiness information (MCAI) states that agent). You are required to assure the product electronically.
there have been: is airworthy before it is returned to service. • Government-wide rulemaking Web
several reports regarding an important (3) Reporting Requirements: For any site: Go to http://www.regulations.gov
corrosion on the bearings with propagation to reporting requirement in this AD, under the and follow the instructions for sending
the bracket-hinge of the rudder. This provisions of the Paperwork Reduction Act your comments electronically.
corrosion has been discovered after rudder (44 U.S.C. 3501 et. seq.), the Office of • Mail: Docket Management Facility;
removals. This condition, if left uncorrected, Management and Budget (OMB) has U.S. Department of Transportation, 400
could result in the loss of the rudder control approved the information collection Seventh Street, SW., Nassif Building,
on the airplane. requirements and has assigned OMB Control Room PL–401, Washington, DC 20590–
Number 2120–0056. 0001.
Actions and Compliance
Related Information • Fax: 1–202–493–2251.
(e) Unless already done, do the following • Hand Delivery: Room PL–401 on
sroberts on PROD1PC70 with PROPOSALS
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8642 Federal Register / Vol. 72, No. 38 / Tuesday, February 27, 2007 / Proposed Rules
association, business, labor union, etc.). a request to examine or copy this 14, Code of Federal Regulations, the
You may review DOT’s complete information, we treat it as any other FAA has reviewed the request made by
Privacy Act Statement in the Federal request under the Freedom of ARSA for extension of the comment
Register published on April 11, 2000 Information Act (5 U.S.C. 552). We period to the Repair Stations, NPRM.
(65 FR 19477–78) or you may visit process such a request under the DOT ARSA has shown a substantive interest
http://dms.dot.gov. procedures found in 49 CFR part 7. in the proposed rule and presented good
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Federal Register / Vol. 72, No. 38 / Tuesday, February 27, 2007 / Proposed Rules 8643
cause for the extension. The FAA also SUMMARY: The Food and Drug agency Web site, as described in the
has determined that extension of the Administration (FDA) is publishing a ADDRESSES portion of this document
comment period is consistent with the proposed rule to reclassify pressure under Electronic Submissions.
public interest, and that good cause regulators for use with medical oxygen, Instructions: All submissions must
exists for taking this action. currently class I devices included in the include the agency name and Docket
Accordingly, the comment period for generic type of device called pressure No. for this rulemaking. All comments
the Repair Stations, NPRM, Docket No. regulator, into class II, subject to special received may be posted without change
FAA–2006–26408, is extended until controls in the form of a guidance to http://www.fda.gov/ohrms/dockets/
April 16, 2007. document. Pressure regulators for use default.htm, including any personal
Issued in Washington, DC, February 20, with all other medical gases will remain information provided. For additional
2007. in class I, subject only to general information on submitting comments,
James J. Ballough, controls. FDA is also proposing to see section XII ‘‘What if I Have
Director, Flight Standards Service, Aviation establish a separate classification Comments to the Proposed Rule’’
Safety. regulation for oxygen conserving heading in the SUPPLEMENTARY
[FR Doc. E7–3331 Filed 2–26–07; 8:45 am] devices (or oxygen conservers), now INFORMATION section of this document.
included in the generic type of device Docket: For access to the docket to
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called noncontinuous ventilator. read background documents or
Oxygen conserving devices will comments received, go to http: //
continue to be classified in class II, but www.fda.gov/ohrms/dockets/
RAILROAD RETIREMENT BOARD default.htm and insert the docket
those that incorporate a built-in oxygen
20 CFR Part 230 pressure regulator will become subject number, found in brackets in the
to the special controls guidance if the heading of this document, into the
RIN 3220–AA61 rule is finalized. Elsewhere in this issue ‘‘Search’’ box and follow the prompts
of the Federal Register, FDA is and/or go to the Division of Dockets
Reduction and Nonpayment of announcing the availability of a class II Management, 5630 Fishers Lane, rm.
Annuities by Reason of Work special controls draft guidance for 1061, Rockville, MD 20852.
AGENCY: Railroad Retirement Board. industry and FDA staff entitled ‘‘Class II FOR FURTHER INFORMATION CONTACT:
ACTION: Proposed rule; withdrawal. Special Controls Guidance Document: Christy Foreman, Center for Devices and
Oxygen Pressure Regulators and Oxygen Radiological Health (HFZ–340), Food
SUMMARY: The above mentioned Conserving Devices.’’ The agency is and Drug Administration, 2094 Gaither
regulation was previously published as proposing this action because it believes Rd., Rockville, MD 20850, 240–276–
a proposed rule on August 16, 1995 (60 that special controls are necessary to 0120.
FR 42482). The Railroad Retirement provide a reasonable assurance of safety
SUPPLEMENTARY INFORMATION:
Board has determined not to go final and effectiveness for these devices.
with that proposed rule and hereby DATES: Submit comments by May 29, I. What Are the Highlights of the
withdraws the proposed rule to amend 2007. FDA is proposing that any final Proposed Rule?
20 CFR Part 230. rule based on this proposed rule be The highlights of the proposed rule
ADDRESSES: 844 North Rush Street, effective 2 years after the date of its are as follows:
Chicago, Illinois 60611–2092. publication in the Federal Register. • FDA is dividing the classification of
FOR FURTHER INFORMATION CONTACT: ADDRESSES: You may submit comments, pressure regulators into two
Marguerite P. Dadabo, Assistant General identified by Docket No. 2007N–0019, classification regulations.
Counsel, Office of General Counsel, by any of the following methods: • Pressure regulators for use with
Railroad Retirement Board, (312) 751– Electronic Submissions medical gases other than oxygen will
4945, FAX (312) 751–7102, TDD (312) Submit electronic comments in the remain in class I.
751–4701. following ways: • Pressure regulators for use with
Dated: February 21, 2007. • Federal eRulemaking Portal: http:// medical oxygen will be identified as
Beatrice Ezerski, www.regulations.gov. Follow the ‘‘oxygen pressure regulators’’ and will
Secretary to the Board. instructions for submitting comments. be reclassified into class II (special
• Agency Web site: http:// controls).
[FR Doc. 07–872 Filed 2–26–07; 8:45 am]
www.fda.gov/dockets/ecomments. • FDA is establishing a separate
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Follow the instructions for submitting classification regulation for oxygen
comments on the agency Web site. conserving devices, which are now
Written Submissions included in the generic type of device
DEPARTMENT OF HEALTH AND Submit written submissions in the called noncontinuous ventilators.
HUMAN SERVICES following ways: • Both noncontinuous ventilators and
• FAX: 301–827–6870. oxygen conserving devices will remain
Food and Drug Administration
• Mail/Hand delivery/Courier [For in class II.
paper, disk, or CD–ROM submissions]: • Oxygen conservers will be classified
21 CFR Part 868
Division of Dockets Management (HFA– within their own class according to
[Docket No. 2007N–0019] 305), Food and Drug Administration, whether or not the device incorporates
5630 Fishers Lane, rm. 1061, Rockville, a built-in oxygen pressure regulator.
Medical Devices; Anesthesiology MD 20852. • FDA is establishing a special
sroberts on PROD1PC70 with PROPOSALS
Devices; Oxygen Pressure Regulators To ensure more timely processing of controls guidance document for oxygen
and Oxygen Conserving Devices comments, FDA is no longer accepting pressure regulators and oxygen
AGENCY: Food and Drug Administration, comments submitted to the agency by e- conservers that have built-in oxygen
HHS. mail. FDA encourages you to continue pressure regulators entitled ‘‘Class II
to submit electronic comments by using Special Controls Guidance Document:
ACTION: Proposed rule.
the Federal eRulemaking Portal or the Oxygen Pressure Regulators and Oxygen
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