ClearanceBrief
510(k) K901143 ยท JBD System, Analysis, Electrophoretic Hemoglobin

REP HEMOGLOBIN IEF KITS (CAT. NO. 3250)

ApplicantHelena Laboratories, Beaumont TX, US
DecisionSubstantially Equivalent, May 23, 1990
ReceivedMar 12, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K901143

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.