510(k) K100654 ยท LDD Dc-Defibrillator, Low-Energy, (Including Paddles)
ZOLL PROPAQ MD
| Applicant | Zoll Medical Corporation, World Wide Headquarters, Chelsmford MA, US |
| Decision | Substantially Equivalent, Jul 29, 2010 |
| Received | Mar 8, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K100654
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.