510(k) K844348 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
DYNASCOPE MONITOR DS-800
| Applicant | Fukuda Denshi USA, Inc., Kirkland WA, US |
| Decision | Substantially Equivalent, Dec 4, 1984 |
| Received | Oct 30, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K844348
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.