510(k) K894460 ยท DSI Detector And Alarm, Arrhythmia
SIEMENS SIRECUST 730, PATIENT MONITOR W/ARRHYTHMIA
| Applicant | Siemens Medical Electronics, Danvers MA, US |
| Decision | Substantially Equivalent, Oct 2, 1989 |
| Received | Jul 18, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K894460
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.