510(k) K862375 ยท DSI Detector And Alarm, Arrhythmia
CARDIO PORT 500 24-H ECG AMBULATORY MONITOR SYSTEM
| Applicant | Grandcor Medical Systems, Dayton OH, US |
| Decision | Substantially Equivalent, Jul 1, 1986 |
| Received | Jun 24, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K862375
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.