ClearanceBrief
510(k) K910232 ยท LLL Extractable Antinuclear Antibody, Antigen And Control

HEMAGEN ENA SCREENING KIT

ApplicantHemagen Diagnostics, Inc., Waltham MA, US
DecisionSubstantially Equivalent, Mar 6, 1991
ReceivedJan 18, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K910232

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.