510(k) K090702 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
MODIFICATION TO DASH 2500 PATIENT MONITOR
| Applicant | Ge Medical Systems Information Technologies, Milwaukee WI, US |
| Decision | Substantially Equivalent, Apr 15, 2009 |
| Received | Mar 17, 2009 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K090702
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.