ClearanceBrief
510(k) K032862 ยท JBD System, Analysis, Electrophoretic Hemoglobin

INTERLAB ALKALINE HEMOGLOBIN ELECTROPHORESIS TEST SYSTEM

ApplicantInterlab S.R.L., East Stroudsburg PA, US
DecisionSubstantially Equivalent, Feb 3, 2004
ReceivedSep 12, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K032862

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.