510(k) K903940 ยท DSI Detector And Alarm, Arrhythmia
TYPE 9210 S/ECG
| Applicant | S & W Medico Teknik, Denmark, DK |
| Decision | Substantially Equivalent, Dec 4, 1991 |
| Received | Aug 27, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K903940
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.