510(k) K895208 ยท DSI Detector And Alarm, Arrhythmia
ZYMED MODEL 1610
| Applicant | Agilent Technologies, Camarillo CA, US |
| Decision | Substantially Equivalent, Dec 12, 1989 |
| Received | Aug 17, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K895208
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.