510(k) K222586 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
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| Applicant | Ge Medical Systems Information Technologies, Inc., Wauwatosa WI, US |
| Decision | Substantially Equivalent, Dec 21, 2022 |
| Received | Aug 26, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K222586
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.