510(k) K792223 ยท DTE Pulse-Generator, Pacemaker, External
PACESETTER MODEL 350
| Applicant | Cynergy, Mchenry IL, US |
| Decision | Substantially Equivalent, Nov 30, 1979 |
| Received | Nov 5, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K792223
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.