510(k) K830013 ยท DSI Detector And Alarm, Arrhythmia
EPI CARDIA SYS. - AMBULATORY MONITOR
| Applicant | Medicomp, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Feb 28, 1983 |
| Received | Jan 3, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K830013
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.