# Medical Devices; Medical Device User Facility and Manufacturer Reporting, Certification and Registration; Office of Management and Budget Approval; Extension of Effective Date
> **Food and Drug Administration** · Final rule; notification of approval of information collection requirements. · Published 1996-04-11 · Effective 1996-07-31 · 61 FR 16043
## Document
- **Document number:** 96-8970
- **Category:** fda-device
- **Sub-agency:** Food and Drug Administration
- **Federal Register citation:** 61 FR 16043
- **CFR reference:** 21 CFR 803
- **Publication date:** 1996-04-11
- **Effective date:** 1996-07-31
- **HHS docket:** Docket No. 91N-0295
## Abstract

The Food and Drug Administration (FDA) is announcing that the Office of Management and Budget (OMB) has approved the collection of information requirements in the final rule on medical device user facility and manufacturer reporting, certification and registration. In addition, FDA is extending to July 31, 1996, the effective date of the final rule in response to requests and in order to allow sufficient time for user facilities and manufacturers to implement procedures to comply with the final rule. The final rule was published in the Federal Register of December 11, 1995 (60 FR 63578).

## Source
- [Federal Register document](https://www.federalregister.gov/documents/1996/04/11/96-8970/medical-devices-medical-device-user-facility-and-manufacturer-reporting-certification-and)
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