510(k) K851517 ยท DSI Detector And Alarm, Arrhythmia
CIRCA MED SINGLE-CHANNEL-AMBULATORY CARDIAC MONITO
| Applicant | Circadian, Inc., San Jose CA, US |
| Decision | Substantially Equivalent, Oct 2, 1985 |
| Received | Apr 15, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K851517
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.