510(k) K951371 ยท DSI Detector And Alarm, Arrhythmia
1481 T DIGITAL TELEMETRY SYSTEM WITH S-T SEGMENT ANALYSIS OPTION
| Applicant | Siemens Medical Solutions USA, Inc., Danvers MA, US |
| Decision | Substantially Equivalent, Oct 4, 1995 |
| Received | Mar 27, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K951371
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.