ClearanceBrief
510(k) K092439 ยท OWB Interventional Fluoroscopic X-Ray System

CANON DIGITAL FLUOROSCOPY AND RADIOGRAPHY, MODEL CXDI-50RF

ApplicantVirtual Imaging, Inc., Deerfield IL, US
DecisionSubstantially Equivalent, Nov 30, 2009
ReceivedAug 10, 2009
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K092439

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.