510(k) K833162 ยท DSI Detector And Alarm, Arrhythmia
AMBULATORY MONITORING DEVICE
| Applicant | Oxford Medilog, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Jan 10, 1984 |
| Received | Sep 16, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K833162
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.