510(k) K802900 ยท DSI Detector And Alarm, Arrhythmia
HEART SENTINEL
| Applicant | Totemite Medical Electronics, Mchenry IL, US |
| Decision | Substantially Equivalent, Mar 11, 1981 |
| Received | Nov 17, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K802900
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.