Legal Status
Legal Status
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
Document Details
Information about this document as published in the Federal Register.
- Printed version:
- 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
-
Enhanced Content - Submit Public Comment
- This feature is not available for this document.
Enhanced Content - Submit Public Comment
-
Enhanced Content - Read Public Comments
Enhanced Content - Read Public Comments
-
Enhanced Content - Sharing
- Shorter Document URL
- https://www.federalregister.gov/d/98-12610 https://www.federalregister.gov/d/98-12610
Enhanced Content - Sharing
-
Enhanced Content - Developer Tools
This document is available in the following developer friendly formats:
More information and documentation can be found in our developer tools pages.
Enhanced Content - Developer Tools
Published Document
This document has been published in the Federal Register. Use the PDF linked in the document sidebar for the official electronic format.
The full text of this document is currently available in PDF format.
The full text of this document is also available in a basic text format.