510(k) K843807 ยท DTE Pulse-Generator, Pacemaker, External
SEAMED MODEL 6000
| Applicant | Seamed Corp., Redmond WA, US |
| Decision | Substantially Equivalent, Feb 1, 1985 |
| Received | Sep 27, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K843807
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.