510(k) K902493 ยท DRI Monitor, Line Isolation
CARDIOCAP II CG-2GS, 2G, 1GS, 1G, 2CG, CS MONITOR
| 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 K902493
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.