510(k) K000746 ยท DSI Detector And Alarm, Arrhythmia
FUKUDA DENSHI DYNASCOPE, MODEL DS-5800NX
| Applicant | Fukuda Denshi USA, Inc., Redmond WA, US |
| Decision | Substantially Equivalent, Apr 7, 2000 |
| Received | Mar 8, 2000 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K000746
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.