ClearanceBrief
510(k) K964806 ยท IXL Device, Spot-Film

MD-1835

ApplicantFischer Imaging Corp., Addison IL, US
DecisionSubstantially Equivalent, Mar 4, 1997
ReceivedNov 29, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K964806

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.