ClearanceBrief
510(k) K961768 ยท LMA Digitizer, Image, Radiological

KODAK DIGITAL SCIENCE FILM DIGITIZER L7501/L7506 (WITH FILM AUTOFEEDER)

ApplicantKodak Health Imaging Systems, Inc., Dallas TX, US
DecisionSubstantially Equivalent, Aug 22, 1996
ReceivedMay 8, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K961768

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.