510(k) K913484 ยท LDD Dc-Defibrillator, Low-Energy, (Including Paddles)
ZOLL D-900 DEFIBRILLATOR
| Applicant | Zmi Corp., Woburn MA, US |
| Decision | Substantially Equivalent, Dec 16, 1991 |
| Received | Aug 6, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K913484
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.