510(k) K211900 · MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
Patient Information Center iX
| Applicant | Philips Medizin Systeme Böblingen GmbH, Boeblingen, DE |
| Decision | Substantially Equivalent, Mar 4, 2022 |
| Received | Jun 21, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K211900
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.