510(k) K934016 ยท DTE Pulse-Generator, Pacemaker, External
POWERCHARGER
| Applicant | Zoll Medical Corp, Burlington MA, US |
| Decision | Substantially Equivalent, Oct 18, 1994 |
| Received | Aug 18, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K934016
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.