510(k) K934254 ยท DRL Tester, Defibrillator
IMPULSE 3000 DEFIBRILLATOR ANALYZER
| Applicant | Dynatech/Nevada, Inc., Washington DC, US |
| Decision | Substantially Equivalent, Nov 23, 1993 |
| Received | Aug 31, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K934254
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.