510(k) K101600 · DQA Oximeter

INTELLIVUE CL SP02 POD MODEL 865215, INTELLIVUE CL NBP POD MODEL 865216, INTELLIVUE PATIENT MONITORS MP5, MP2, X2 MODEL

Applicant	Philips Medizinsysteme Boeblingen GmbH, Cardiac AN, Boeblingen, Baden-Wuerttemberg, DE
Decision	Substantially Equivalent, Aug 31, 2010
Received	Jun 8, 2010
Type	Abbreviated
FDA record	Open on fda.gov

Recalls that name K101600

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.