510(k) K980625 ยท DSI Detector And Alarm, Arrhythmia
SIEMENS MULTIVIEW WORKSTATION ENHANCED WITH DIAGNOSTIC STATEMENTS (REST ECG)
| Applicant | Siemens Medical Solutions USA, Inc., Danvers MA, US |
| Decision | Substantially Equivalent, May 19, 1998 |
| Received | Feb 18, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K980625
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.