Regulations.gov document
Cardiovascular Devices; Reclassification of External Pacemaker Pulse Generator Devices…
Proposed Rule · FDA-2011-N-0650 · posted Sep 15, 2014
Key facts
| Document ID | FDA-2011-N-0650-0006 |
|---|---|
| Title | Cardiovascular Devices; Reclassification of External Pacemaker Pulse Generator Devices; Reclassification of Pacing System Analyzers |
| Document type | Proposed Rule |
| Subtype | Notice of Proposed Rulemaking (NPRM) |
| Agency | FDA |
| Docket | FDA-2011-N-0650 |
| Posted | Sep 15, 2014 |
| Federal Register citation | 79 FR 54927 |
| FR document number | 2014-21814 |
| CFR | 21 CFR Part 870 |
| Comment period opens | Sep 15, 2014 |
| Comments due | Dec 16, 2014 |
| Effective date | Sep 15, 2014 |
At a glance
- 10–99 Pages
- No Open for comment
- 1–9 Public comments on this docket
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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