510(k) K812317 ยท LDD Dc-Defibrillator, Low-Energy, (Including Paddles)
DEFIBRILLATOR/MONITOR
| Applicant | Hewlett-Packard Co., Mchenry IL, US |
| Decision | Substantially Equivalent, Sep 21, 1981 |
| Received | Aug 17, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K812317
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.