510(k) K802033 ยท DSI Detector And Alarm, Arrhythmia
OXFORD INTENSIVE CARE PATIENT MON. SYS
| Applicant | Oxford Medilog, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Sep 26, 1980 |
| Received | Aug 22, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K802033
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.