510(k) K852207 ยท DSI Detector And Alarm, Arrhythmia
OXFORD VDT-40 DISPLAY TERMINAL
| Applicant | Oxford Medilog, Inc., Clearwater FL, US |
| Decision | Substantially Equivalent, Jun 11, 1985 |
| Received | May 21, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K852207
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.