510(k) K912188 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
DINAMAP PLUS PHYSIOLOGICAL MONITOR MODEL 8700
| Applicant | Critikon Company, LLC, Tampa FL, US |
| Decision | Substantially Equivalent, Dec 4, 1991 |
| Received | May 17, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K912188
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.