510(k) K874768 ยท DSI Detector And Alarm, Arrhythmia
FUKUDA DENSHI MODEL FCP-231
| Applicant | Fukuda Denshi USA, Inc., Kirkland WA, US |
| Decision | Substantially Equivalent, Dec 18, 1987 |
| Received | Nov 19, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K874768
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.