510(k) K902478 ยท LDD Dc-Defibrillator, Low-Energy, (Including Paddles)
LIFEPAK 300 AUTOMATIC ADVISORY DEFIBRILLATOR
| Applicant | Physio-Control Corp., Redmond WA, US |
| Decision | Substantially Equivalent, Oct 31, 1990 |
| Received | Jun 4, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K902478
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.