510(k) K900607 ยท DSI Detector And Alarm, Arrhythmia
MK5 DETECTOR & ALARM, ARRHYTHMIA W/SOFTWARE 2.11
| Applicant | Cardiodata Corp., Northborough MA, US |
| Decision | Substantially Equivalent, Oct 16, 1990 |
| Received | Feb 8, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K900607
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.