510(k) K883930 ยท DTE Pulse-Generator, Pacemaker, External
SEAMED MODEL 3300 DUAL CHAMBER PACING SYSTEM ANALY
| Applicant | Seamed Corp., Bothell WA, US |
| Decision | Substantially Equivalent, Nov 9, 1988 |
| Received | Sep 15, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K883930
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.