ClearanceBrief
510(k) K791791 ยท KSG Media, Potentiating For In Vitro Diagnostic Use

ORTHO ANTIBODY ENHANCEMENT SOLUTION

ApplicantOrtho Diagnostics, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Oct 11, 1979
ReceivedSep 11, 1979
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K791791

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.