ClearanceBrief
510(k) K860777 ยท LMA Digitizer, Image, Radiological

MATRIX LD & LD/LASER DIGITIZER

ApplicantMatrix Instruments, Orangeburg NY, US
DecisionSubstantially Equivalent, Apr 22, 1987
ReceivedMar 3, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K860777

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.