510(k) K230604 · MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)

IntelliVue Patient Monitor MX100 (867033), IntelliVue Multi-Measurement Module X3 (867030)

Applicant	Philips Medizin Systeme Boeblingen GmbH, Böblingen, DE
Decision	Substantially Equivalent, Nov 22, 2023
Received	Mar 3, 2023
Type	Traditional
FDA record	Open on fda.gov

Recalls that name K230604

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.