510(k) K092680 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
DATEX-OHMEDA S/5 ANESTHESIA MONITOR WITH L-ANEO7 AND L-ANEO7A SOFTWARE USING F-CU8 OR F-CU5 (P) MONITOR FRAME OPTIONS AN
| Applicant | GE Healthcare Finland Oy, Helsinki, FI |
| Decision | Substantially Equivalent, Sep 23, 2009 |
| Received | Sep 1, 2009 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K092680
No recall in the FDA data names this 510(k).
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