510(k) K911402 ยท LDD Dc-Defibrillator, Low-Energy, (Including Paddles)
MODEL #350 SHOCK-PLATE DEFIB ADAPTOR
| Applicant | Cardiotronics, Inc., West Carlsbad CA, US |
| Decision | Substantially Equivalent, Oct 3, 1991 |
| Received | Mar 29, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K911402
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.