ClearanceBrief
510(k) K810355 ยท CKA Nadh Oxidation/Nad Reduction, Alt/Sgpt

ALT (UV) TEST

ApplicantBoehringer Mannheim Corp., Walker MI, US
DecisionSubstantially Equivalent, Feb 23, 1981
ReceivedFeb 10, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K810355

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.