510(k) K854648 ยท DTE Pulse-Generator, Pacemaker, External
SEAMED MODEL 4000
| Applicant | Seamed Corp., Redmond WA, US |
| Decision | Substantially Equivalent, Jan 16, 1986 |
| Received | Nov 19, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K854648
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.