510(k) K832827 ยท LDD Dc-Defibrillator, Low-Energy, (Including Paddles)
CORPULS 300
| Applicant | Automated Medical Products, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Nov 3, 1983 |
| Received | Aug 22, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K832827
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.