510(k) K903514 ยท DSI Detector And Alarm, Arrhythmia
FUKUDA DENSHI MODEL LX-3100
| Applicant | Fukuda Denshi USA, Inc., Redmond WA, US |
| Decision | Substantially Equivalent, Jan 30, 1991 |
| Received | Aug 3, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K903514
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.