ClearanceBrief
510(k) K915058 ยท LLL Extractable Antinuclear Antibody, Antigen And Control

HEMAGEN ENA SCREENING KIT (EIA METHOD)

ApplicantHemagen Diagnostics, Inc., Waltham MA, US
DecisionSubstantially Equivalent, Dec 20, 1991
ReceivedNov 8, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K915058

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.