510(k) K896417 ยท DPS Electrocardiograph
KONTRON KOLORMON 7250 PATIENT MONITOR
| Applicant | Kontron Instruments, Inc., Everett MA, US |
| Decision | Substantially Equivalent, Dec 12, 1989 |
| Received | Nov 8, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K896417
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.