ClearanceBrief
510(k) K810598 ยท IZW Collimator, Automatic, Radiographic

X-RAY COLLIMATING DEVICES

ApplicantMidmark Corp., Versailles OH, US
DecisionSubstantially Equivalent, Apr 10, 1981
ReceivedMar 6, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K810598

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.