ClearanceBrief
510(k) K993598 ยท LMA Digitizer, Image, Radiological

MAMMOGRAPHY PRO, MODEL 13017, DIAGNOSTIC PRO W/ MAMMOGRAPHY OPTION, MODEL 13205

ApplicantVidar Systems Corp., Herndon VA, US
DecisionSubstantially Equivalent, Jan 20, 2000
ReceivedOct 25, 1999
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K993598

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.