510(k) K031376 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
DINAMAP PRO 1000 V3 MONITOR, MODEL 1100 SERIES
| Applicant | Ge Medical Systems Information Technologies, Tampa FL, US |
| Decision | Substantially Equivalent, Jul 16, 2003 |
| Received | May 1, 2003 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K031376
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.