510(k) K802221 ยท DTE Pulse-Generator, Pacemaker, External
CHRONOCOR IV MODEL 250
| Applicant | Cordis Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Nov 19, 1980 |
| Received | Sep 12, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K802221
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.