ClearanceBrief
510(k) K970908 ยท LMA Digitizer, Image, Radiological

HOWTEK 960

ApplicantHowtek, Inc., Hudson NH, US
DecisionSubstantially Equivalent, May 20, 1997
ReceivedMar 11, 1997
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K970908

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.