View Information Collection Request (ICR) Package
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Please note that the OMB number and expiration date may not have been determined when this Information Collection Request and associated Information Collection forms were submitted to OMB. The approved OMB number and expiration date may be found by clicking on the Notice of Action link below.
View ICR - OIRA Conclusion
OMB Control No:
2120-0702
ICR Reference No:
201605-2120-005
Status:
Historical Inactive
Previous ICR Reference No:
201410-2120-002
Agency/Subagency:
DOT/FAA
Agency Tracking No:
Final Rule
Title:
Use of Certain Personal Oxygen Concentrator (POC) Devices on Board Aircraft
Type of Information Collection:
Extension without change of a currently approved collection
Common Form ICR:
No
Type of Review Request:
Regular
OIRA Conclusion Action:
Comment filed on proposed rule and continue
Conclusion Date:
09/08/2016
Retrieve Notice of Action (NOA)
Date Received in OIRA:
05/31/2016
Terms of Clearance:
The agency will respond to comments in the final rule.
Inventory as of this Action
Requested
Previously Approved
Expiration Date
05/31/2016
4 Months From Approved
09/30/2016
Responses
722,455
0
722,455
Time Burden (Hours)
72,142
0
72,142
Cost Burden (Dollars)
0
0
0
Abstract:
The rule requires passengers who intend to use an approved POC to present a physician statement before boarding. The flight crew must then inform the pilot-in-command that a POC is on board. This request will be withdrawn when the Final Rule is effective approximately June 2016. The Final Rule, 2120-AK32 - Personal Oxygen Concentrator (POC) Devices will remove the FAA's requirement to collect this information.
Authorizing Statute(s):
US Code:
49 USC 44701
Name of Law: General requirements
Citations for New Statutory Requirements:
None
Associated Rulemaking Information
RIN:
Stage of Rulemaking:
Federal Register Citation:
Date:
2120-AK32
Proposed rulemaking
79 FR 56305
09/19/2014
Federal Register Notices & Comments
Did the Agency receive public comments on this ICR?
No
Number of Information Collection (IC) in this ICR:
2
IC Title
Form No.
Form Name
Use of Certain Personal Oxygen Concentrator (POC) Devices on Board Aircraft - Flight Crew
Use of Certain Personal Oxygen Concentrator (POC) Devices on Board Aircraft - Physicians
Burden increases because of Program Change due to Agency Discretion:
No
Burden Increase Due to:
Burden decreases because of Program Change due to Agency Discretion:
Yes
Burden Reduction Due to:
Changing Regulations
Short Statement:
The burden and costs for completion of physician’s statements and flight crew notification have been revised based on a 4 month collection time-frame. The publication of 2120-AK32, Acceptance Criteria of Portable Oxygen Concentrators Used On Board Aircraft (79FR56303), eliminates the requirement to collect this information so it will be withdrawn after 4 months.
Annual Cost to Federal Government:
$0
Does this IC contain surveys, censuses, or employ statistical methods?
No
Is the Supporting Statement intended to be a Privacy Impact Assessment required by the E-Government Act of 2002?
No
Is this ICR related to the Affordable Care Act [Pub. L. 111-148 & 111-152]?
No
Is this ICR related to the Dodd-Frank Wall Street Reform and Consumer Protection Act, [Pub. L. 111-203]?
No
Is this ICR related to the American Recovery and Reinvestment Act of 2009 (ARRA)?
No
Is this ICR related to the Pandemic Response?
Uncollected
Agency Contact:
Denise Deaderick 202 267-8166 dk.deaderick@faa.gov
Common Form ICR:
No
On behalf of this Federal agency, I certify that the collection of information encompassed by this request complies with 5 CFR 1320.9 and the related provisions of 5 CFR 1320.8(b)(3).
The following is a summary of the topics, regarding the proposed collection of information, that the certification covers:
(a) It is necessary for the proper performance of agency functions;
(b) It avoids unnecessary duplication;
(c) It reduces burden on small entities;
(d) It uses plain, coherent, and unambiguous language that is understandable to respondents;
(e) Its implementation will be consistent and compatible with current reporting and recordkeeping practices;
(f) It indicates the retention periods for recordkeeping requirements;
(g) It informs respondents of the information called for under 5 CFR 1320.8 (b)(3) about:
(i) Why the information is being collected;
(ii) Use of information;
(iii) Burden estimate;
(iv) Nature of response (voluntary, required for a benefit, or mandatory);
(v) Nature and extent of confidentiality; and
(vi) Need to display currently valid OMB control number;
(h) It was developed by an office that has planned and allocated resources for the efficient and effective management and use of the information to be collected.
(i) It uses effective and efficient statistical survey methodology (if applicable); and
(j) It makes appropriate use of information technology.
If you are unable to certify compliance with any of these provisions, identify the item by leaving the box unchecked and explain the reason in the Supporting Statement.
Certification Date:
05/31/2016
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