510(k) K860767 ยท DSI Detector And Alarm, Arrhythmia
MODEL E 600 ELECTROCARDIOGRAPH
| Applicant | Kone Instruments, Inc., Milton WI, US |
| Decision | Substantially Equivalent, Apr 23, 1986 |
| Received | Mar 3, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K860767
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.