ClearanceBrief
510(k) K983914 ยท GGP Test, Qualitative And Quantitative Factor Deficiency

REAADS MONOCLONAL FREE PROTEIN S ANTIGEN TEST KIT

ApplicantCorgenix, Inc., Westminster CO, US
DecisionSubstantially Equivalent, Dec 22, 1998
ReceivedNov 4, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K983914

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.