510(k) K810940 ยท DSI Detector And Alarm, Arrhythmia
THE BETA
| Applicant | Burdick Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Jul 16, 1981 |
| Received | Apr 7, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K810940
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.