510(k) K897080 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
CARDIOCAP(TM) CT-104 MONITOR
| Applicant | Datex Division Instrumentarium Corp., Helsinki, Finland, FI |
| Decision | Substantially Equivalent, Mar 6, 1990 |
| Received | Dec 21, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K897080
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.