510(k) K880780 ยท DRL Tester, Defibrillator
HEARTSTART 2000 DEFIBRILLATOR TESTER, ECG
| Applicant | First Medical Devices Corp., Bellevue WA, US |
| Decision | Substantially Equivalent, May 12, 1988 |
| Received | Feb 26, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880780
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.