510(k) K812586 ยท LDD Dc-Defibrillator, Low-Energy, (Including Paddles)
KANTRON 504 HEARTSTATION
| Applicant | Kantron Cardiovascular, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Dec 29, 1981 |
| Received | Sep 11, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K812586
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.