510(k) K014255 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
DINAMAP PROCARE SERIES MONITOR; MODEL 100, 200, 300, 400
| Applicant | Ge Medical Systems Information Technologies, Tampa FL, US |
| Decision | Substantially Equivalent, Jul 2, 2002 |
| Received | Dec 26, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K014255
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.