510(k) K902492 ยท DRI Monitor, Line Isolation
CARDIOCAP II MONITORS: CH, CH-2, CH-S, CH-2S
| Applicant | Datex Division Instrumentarium Corp., Helsinki, Finland, FI |
| Decision | Substantially Equivalent, Jul 6, 1990 |
| Received | Jun 5, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K902492
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.