510(k) K883617 ยท LDD Dc-Defibrillator, Low-Energy, (Including Paddles)
LIFEPAK 50 MONITOR/DEFIBRILLATOR
| Applicant | Physio-Control Corp., Redmond WA, US |
| Decision | Substantially Equivalent, Dec 28, 1988 |
| Received | Aug 24, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K883617
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.