510(k) K963190 ยท DRL Tester, Defibrillator
QA-40M DEFIBRILLATOR TESTER
| Applicant | Metron U.S., Inc., Grand Rapids MI, US |
| Decision | Substantially Equivalent, Jul 1, 1997 |
| Received | Aug 15, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K963190
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.