510(k) K821791 ยท DTE Pulse-Generator, Pacemaker, External
EXTERNAL PULSE GENERATOR - EV4542
| Applicant | American Pacemaker Corp., Walker MI, US |
| Decision | Substantially Equivalent, Jul 6, 1982 |
| Received | Jun 17, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K821791
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.