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Proposed Rule

Medical Device Reporting: Manufacturer Reporting, Importer Reporting, User Facility Reporting, and Distributor Reporting; Companion Document to Direct Final Rule

A Proposed Rule by the Food and Drug Administration on 05/12/1998

Document Details

Information about this document as published in the Federal Register.

Printed version:
PDF
Publication Date:
05/12/1998
Agencies:
Food and Drug Administration
Dates:
Submit written comments on or before July 27, 1998. Submit written comments on the information collection requirements on or before July 13, 1998.
Comments Close:
07/27/1998
Document Type:
Proposed Rule
Document Citation:
63 FR 26129
Page:
26129-26137 (9 pages)
CFR:
21 CFR 803
21 CFR 804
Agency/Docket Number:
Docket No. 98N-0170
Document Number:
98-12610
Document Details
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