510(k) K852250 ยท DSI Detector And Alarm, Arrhythmia
595 ARRHYTHMIA MONITORING SYSTEM
| Applicant | Burdick Corp., Miltoon WI, US |
| Decision | Substantially Equivalent, May 2, 1986 |
| Received | May 23, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K852250
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.