510(k) K844791 ยท DSI Detector And Alarm, Arrhythmia
SYSTEM SIRECUST 400 SIEMENS SIRECUST 456-1A
| Applicant | Analogic Corp., Peabody MA, US |
| Decision | Substantially Equivalent, Apr 10, 1985 |
| Received | Dec 10, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K844791
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.