510(k) K890330 ยท DSI Detector And Alarm, Arrhythmia
MEDILOG 6000-FD REPORT GENERATOR
| Applicant | Oxford Medilog, Inc., Clearwater FL, US |
| Decision | Substantially Equivalent, Apr 20, 1989 |
| Received | Jan 23, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890330
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.