510(k) K911604 ยท LDD Dc-Defibrillator, Low-Energy, (Including Paddles)
MDPHONE CELLULAR + RESCUE (DEFIB SYSTEM)
| Applicant | Medphone Corp., Paramus NJ, US |
| Decision | Substantially Equivalent, Sep 23, 1991 |
| Received | Apr 10, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K911604
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.