510(k) K882513 ยท DSI Detector And Alarm, Arrhythmia
MODIFIED HEART*AID 97 AUTO. EXTERNAL DEFIBRILLATOR
| Applicant | Cardiac Resucitator Corp., Portland OR, US |
| Decision | Substantially Equivalent, Jul 12, 1988 |
| Received | Jun 2, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K882513
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.