510(k) K893405 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
MODEL DS-504 DYNASCOPE PATIENT MONITOR
| Applicant | Fukuda Denshi USA, Inc., Redmond WA, US |
| Decision | Substantially Equivalent, Oct 2, 1989 |
| Received | May 2, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K893405
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.