510(k) K050762 · MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)

PHILIPS INTELLIVUE PATIENT MONITOR, MODELS MP20, MP30, MP40, MP50, MP60, MP70 AND MP90

Applicant	Philips Medizin Systeme Boeblingen GmbH, Boeblingen, Bw, DE
Decision	Substantially Equivalent, Apr 22, 2005
Received	Mar 24, 2005
Type	Special
FDA record	Open on fda.gov

Recalls that name K050762

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.