ClearanceBrief
510(k) K925721 ยท LMA Digitizer, Image, Radiological

KODAK EKTASCAN CP PRIMARY HIGH FREQ. VID.INTERFACE

ApplicantEastman Kodak Company, Rochester NY, US
DecisionSubstantially Equivalent, Feb 26, 1993
ReceivedNov 12, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K925721

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.