510(k) K897074 ยท DSI Detector And Alarm, Arrhythmia
MODEL 215M PATIENT SIMULATOR
| Applicant | Dynatech/Nevada, Inc., Carson City NV, US |
| Decision | Substantially Equivalent, May 17, 1990 |
| Received | Dec 22, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K897074
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.