510(k) K923621 ยท DTE Pulse-Generator, Pacemaker, External
EXTERNAL DEMAND PACEMAKER
| Applicant | Oscor Medical Corp., Palm Harbor FL, US |
| Decision | Substantially Equivalent, May 19, 1993 |
| Received | Jul 21, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K923621
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.