510(k) K871251 ยท DSI Detector And Alarm, Arrhythmia
CIRCAMED FULL DISCLOSURE SYSTEM
| Applicant | Circadian, Inc., San Jose CA, US |
| Decision | Substantially Equivalent, May 22, 1987 |
| Received | Mar 30, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K871251
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.