510(k) K903704 ยท DSI Detector And Alarm, Arrhythmia
FUKUDA DENSHI MODEL FCP-2201 MODIFICATION
| Applicant | Fukuda Denshi USA, Inc., Redmond WA, US |
| Decision | Substantially Equivalent, Sep 7, 1990 |
| Received | Jun 12, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K903704
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.