510(k) K221348 · MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)

IntelliVue Patient Monitor MX750 (866471);IntelliVue Patient Monitor MX850 (866470)

Applicant	Philips Medizin Systeme Böblingen GmbH, Boeblingen, DE
Decision	Substantially Equivalent, Feb 3, 2023
Received	May 9, 2022
Type	Traditional
FDA record	Open on fda.gov

Recalls that name K221348

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.