510(k) K111905 · DXJ Display, Cathode-Ray Tube, Medical

INTELLIVUE GUARDIAN SOFTWARE MODEL 866009, INTELLIVUE CL SP02 POD MODEL 865215, INTELLIVUE CL NBP POD MODEL 865216

Applicant	Philips Medizinsysteme Boeblingen GmbH, Cardiac AN, Boeblingen, Baden-Wuerttemberg, DE
Decision	Substantially Equivalent, Oct 4, 2011
Received	Jul 5, 2011
Type	Abbreviated
FDA record	Open on fda.gov

Recalls that name K111905

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.