510(k) K022834 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
DINAMAP PRO 1000 MONITOR WITH SUPERSTAT, MODEL 1000
| Applicant | Ge Medical Systems Information Technologies, Tampa FL, US |
| Decision | Substantially Equivalent, May 13, 2003 |
| Received | Aug 26, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K022834
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.