ClearanceBrief
510(k) K020243 ยท LMA Digitizer, Image, Radiological

LASERPRO 16

ApplicantEradlink, Inc., Penn Valley CA, US
DecisionSubstantially Equivalent, Mar 5, 2002
ReceivedJan 23, 2002
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K020243

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.