510(k) K860462 ยท DTC Analyzer, Pacemaker Generator Function
SEAMED MODEL 3000
| Applicant | Seamed Corp., Redmond WA, US |
| Decision | Substantially Equivalent, Aug 19, 1986 |
| Received | Feb 6, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K860462
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.