510(k) K140502 ยท LDD Dc-Defibrillator, Low-Energy, (Including Paddles)
ZOLL E SERIES ALS
| Applicant | ZOLL Medical Corporation, Chelsmford MA, US |
| Decision | Substantially Equivalent, Nov 6, 2014 |
| Received | Feb 27, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K140502
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.