510(k) K921765 ยท LDD Dc-Defibrillator, Low-Energy, (Including Paddles)
PRIMEDIC DEFIBRILLATORS-N/B
| Applicant | Metronic Electronic GmbH, Hampton VA, US |
| Decision | Substantially Equivalent, Mar 3, 1993 |
| Received | Apr 14, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K921765
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.