510(k) K843229 ยท LDD Dc-Defibrillator, Low-Energy, (Including Paddles)
LIFEPAK 200
| Applicant | Physio-Control Corp., Redmond WA, US |
| Decision | Substantially Equivalent, Oct 18, 1984 |
| Received | Aug 17, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K843229
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.