510(k) K883410 ยท DSI Detector And Alarm, Arrhythmia
CARDIOMEGA-T
| Applicant | Grandcor Medical Systems, Dayton OH, US |
| Decision | Substantially Equivalent, Oct 17, 1988 |
| Received | Aug 11, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K883410
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.