510(k) K872551 ยท DTE Pulse-Generator, Pacemaker, External
SEAMED MODEL 3200
| Applicant | Seamed Corp., Bothell WA, US |
| Decision | Substantially Equivalent, Jul 31, 1987 |
| Received | Jun 29, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K872551
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.