510(k) K020084 ยท DSI Detector And Alarm, Arrhythmia
FUKUDA DENSHI DYNASCOPE MODEL DS-5700
| Applicant | Fukuda Denshi USA, Inc., Redmond WA, US |
| Decision | Substantially Equivalent, Feb 6, 2002 |
| Received | Jan 10, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K020084
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.