510(k) K904159 ยท DRL Tester, Defibrillator
DEFIBRILLATOR ANALYZER MODEL QED-5
| Applicant | Bio-Tek Instruments, Inc., Winooski VT, US |
| Decision | Substantially Equivalent, Mar 18, 1991 |
| Received | Sep 11, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K904159
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.