ClearanceBrief
510(k) K020241 ยท MID System, Test, Anticardiolipin Immunological

QACA IGG/IGM ELISA KIT

ApplicantCheshire Diagnostics , Ltd., Cheshire, GB
DecisionSubstantially Equivalent, Mar 13, 2002
ReceivedJan 23, 2002
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K020241

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.