510(k) K895547 ยท DSI Detector And Alarm, Arrhythmia
GRANDCOR/CARDIOLINE ECT STRESS TESTING
| Applicant | Grandcor Medical Systems, Dayton OH, US |
| Decision | Substantially Equivalent, Mar 13, 1990 |
| Received | Sep 13, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K895547
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.