Oxygen Consumer Survey: Medical Equipment and Supplies Consumer Survey

Forms and Documents

Document Name	Status

No forms / supporting documents in this ICR. Check IC Document Collections.

IC Document Collections

IC ID	Document Title	Status
8594	Oxygen Consumer Survey: Medical Equipment and Supplies Consumer Survey Form	Migrated

ICR Details

OMB Control No: 0938-0807	ICR Reference No: 200105-0938-008
Status: Historical Active	Previous ICR Reference No: 200008-0938-002
Agency/Subagency: HHS/CMS	Agency Tracking No:
Title: Oxygen Consumer Survey: Medical Equipment and Supplies Consumer Survey
Type of Information Collection: Reinstatement with change of a previously approved collection	Common Form ICR:  No
Type of Review Request: Regular
OIRA Conclusion Action: Approved without change	Conclusion Date: 07/30/2001
	Date Received in OIRA: 05/31/2001
Terms of Clearance: OMB approves this instrument for use in San Antonio, Tx. and other sites selected for the DME Competitive Bidding Demonstra- tion. However, any site-specific revisions to this instrument or the underlying sampling or survey methodologies must be submitted for OMB PRA review prior to implementation. In addition CMS promptly must submit to OMB correction worksheets updating the burden and respondents involved in this demonstration.

	Inventory as of this Action	Requested	Previously Approved
Expiration Date	12/31/2002	12/31/2002
Responses	2,500	0	0
Time Burden (Hours)	725	0	0
Cost Burden (Dollars)	0	0	0

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Abstract: This survey is necessary to collect access, quality, and diversity of product selection information from beneficiaries. These key elements of the evaluation cannot be thoroughly evaluated without a beneficiary survey. The information will be presented to HCFA and to Congress, who will use the results to determine whether the demonstration should be extended to other sites. The respondents will be Medicare beneficiaries, that is, those who are age 65 or older or are disabled. These beneficiaries qualify for the survey if they use at least one of the following types of medical equipment: hospital beds,.......

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Authorizing Statute(s): None

Citations for New Statutory Requirements: None

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Associated Rulemaking Information
RIN:	Stage of Rulemaking:	Federal Register Citation:	Date:

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Federal Register Notices & Comments

Did the Agency receive public comments on this ICR? No

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Number of Information Collection (IC) in this ICR: 1

IC Title	Form No.	Form Name
Oxygen Consumer Survey: Medical Equipment and Supplies Consumer Survey	HCFA-10016

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ICR Summary of Burden

	Total Approved	Previously Approved	Change Due to New Statute	Change Due to Agency Discretion	Change Due to Adjustment in Estimate	Change Due to Potential Violation of the PRA
Annual Number of Responses	2,500	0	0	2,500	0	0
Annual Time Burden (Hours)	725	0	0	725	0	0
Annual Cost Burden (Dollars)	0	0	0	0	0	0

Burden increases because of Program Change due to Agency Discretion: Yes

Burden Increase Due to:

Burden decreases because of Program Change due to Agency Discretion: No

Burden Reduction Due to:

Short Statement:

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Annual Cost to Federal Government: $0

Does this IC contain surveys, censuses, or employ statistical methods? Yes Part B of Supporting Statement

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]? Uncollected

Is this ICR related to the Dodd-Frank Wall Street Reform and Consumer Protection Act, [Pub. L. 111-203]? Uncollected

Is this ICR related to the American Recovery and Reinvestment Act of 2009 (ARRA)? Uncollected

Is this ICR related to the Pandemic Response? Uncollected

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Common Form ICR:  No

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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: 05/31/2001

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