510(k) K931803 ยท LDD Dc-Defibrillator, Low-Energy, (Including Paddles)
5200 ADULT SOLID GEL MULTI-FUNCTION ELECTRODES
| Applicant | Zoll Medical Corp, Burlington MA, US |
| Decision | Substantially Equivalent, Oct 8, 1993 |
| Received | Apr 12, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K931803
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.