510(k) K952054 ยท DSI Detector And Alarm, Arrhythmia
SIEMENS SIRECUST MONITORING (1200, 1200 NEO, 960)
| Applicant | Siemens Medical Solutions USA, Inc., Danvers MA, US |
| Decision | Substantially Equivalent, Jun 7, 1996 |
| Received | May 1, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K952054
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.