510(k) K944350 ยท DSI Detector And Alarm, Arrhythmia
SC 6000/ SC 6000P/ R50
| Applicant | Siemens Medical Solutions USA, Inc., Danvers MA, US |
| Decision | Substantially Equivalent, Apr 10, 1995 |
| Received | Sep 6, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K944350
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.