510(k) K103651 ยท LDD Dc-Defibrillator, Low-Energy, (Including Paddles)
CARDIOMED
| Applicant | Cardio Medical Products, Inc., Rockaway NJ, US |
| Decision | Substantially Equivalent, Oct 4, 2011 |
| Received | Dec 14, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K103651
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.