510(k) K863903 ยท DTE Pulse-Generator, Pacemaker, External
SEA MED MODEL 6000
| Applicant | Seamed Corp., Bothell WA, US |
| Decision | Substantially Equivalent, Dec 10, 1986 |
| Received | Oct 7, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K863903
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.