510(k) K864401 ยท DSI Detector And Alarm, Arrhythmia
PLURIMUS CARDIAC EVALUATION SYSTEM
| Applicant | Vivix Corp., San Jose CA, US |
| Decision | Substantially Equivalent, Mar 3, 1987 |
| Received | Nov 6, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K864401
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.