ClearanceBrief
510(k) K040146 ยท GKA Abnormal Hemoglobin Quantitation

INTERLAB ACID HEMOGLOBIN ELECTROPHORESIS TEST SYSTEM

ApplicantInterlab S.R.L., East Stroudsburg PA, US
DecisionSubstantially Equivalent, May 4, 2004
ReceivedJan 22, 2004
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K040146

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.