REPORTING AND RECORDKEEPING REQUIREMENTS FOR ELECTRONIC PRODUCTS UNDER PUBLIC LAW 90-602-GENERAL REQUIREMENTS

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
109379	REPORTING AND RECORDKEEPING REQUIREMENTS FOR ELECTRONIC PRODUCTS UNDER PUBLIC LAW 90-602-GENERAL REQUIREMENTS Form	Migrated

ICR Details

OMB Control No: 0910-0025	ICR Reference No: 198807-0910-002
Status: Historical Active	Previous ICR Reference No: 198506-0910-006
Agency/Subagency: HHS/FDA	Agency Tracking No:
Title: REPORTING AND RECORDKEEPING REQUIREMENTS FOR ELECTRONIC PRODUCTS UNDER PUBLIC LAW 90-602-GENERAL REQUIREMENTS
Type of Information Collection: Revision of a currently approved collection	Common Form ICR:  No
Type of Review Request: Regular
OIRA Conclusion Action: Approved without change	Conclusion Date: 10/20/1988
	Date Received in OIRA: 07/27/1988
Terms of Clearance: This information collection request is granted a short term clearance subject to the following: Pursuant to 5 CFR 1320.14, OMB is notifying FDA to initiate a proposal to exempt from the 5 year recordkeeping requirement under 21 CFR 1002.40 all or most non-ionizing electronic products. FDA has not demonstrated either a need for or the practical utility of this requirement for these products, particularly in light of the absence of risk and incidents involving these products.

	Inventory as of this Action	Requested	Previously Approved
Expiration Date	04/30/1989	04/30/1989	08/31/1988
Responses	41,601	0	41,882
Time Burden (Hours)	1,385,691	0	1,466,783
Cost Burden (Dollars)	0	0	0

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Abstract: THE PURPOSE OF THE RADIATION CONTROL FOR HEALTH AND SAFETY ACT IS TO PROTE THE PUBLIC FROM UNNECESSARY EXPOSURE TO RADIATION FROM ELECTRONIC PRODUCTS. TO CARRY OUT THIS RESPONSIBILITY, FDA MUST COLLECT CERTAIN INFORMATION FROM THE MANUFACTURERS AND DEALER/DISTRIBUTORS ABOUT THE ELECTRONIC PRODUCTS THEY SELL AND INSTALL. THIS REQUEST CONTAINS SEVERAL TYPES OF INFORMATION COLLECTIONS AND RECORDKEEPING REQUIREMENT

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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
REPORTING AND RECORDKEEPING REQUIREMENTS FOR ELECTRONIC PRODUCTS UNDER PUBLIC LAW 90-602-GENERAL REQUIREMENTS	FDA 766, 2877 & 3147

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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	41,601	41,882	0	-281	0	0
Annual Time Burden (Hours)	1,385,691	1,466,783	0	-81,092	0	0
Annual Cost Burden (Dollars)	0	0	0	0	0	0

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:

Short Statement:

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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]? 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: 07/27/1988

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