ClearanceBrief
510(k) K130406 ยท LMA Digitizer, Image, Radiological

DIAGNOSTICPRO EDGE

ApplicantVidar Systems Corp., Herndon VA, US
DecisionSubstantially Equivalent, Apr 29, 2013
ReceivedFeb 19, 2013
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K130406

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.