510(k) K904355 ยท DPS Electrocardiograph
CARDIOCAP II TM CH-RESP MONITORS
| Applicant | Instrumentarium Corp., Finland, FI |
| Decision | Substantially Equivalent, May 23, 1991 |
| Received | Sep 24, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K904355
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.