510(k) K992638 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
DINAMAP PRO SERIES MONITOR, MODELS 100, 200, 300, 400
| Applicant | Critikon Company, LLC, Tampa FL, US |
| Decision | Substantially Equivalent, Feb 24, 2000 |
| Received | Aug 6, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K992638
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.