510(k) K840055 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
DYNASCOPE SERIES
| Applicant | Fukuda Denshi USA, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Aug 22, 1984 |
| Received | Jan 6, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K840055
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.