ClearanceBrief
510(k) K792335 ยท GGP Test, Qualitative And Quantitative Factor Deficiency

HELENA FACTOR VIII DEFICIENT SUB. PLASMA

ApplicantHelena Laboratories, Mchenry IL, US
DecisionSubstantially Equivalent, Dec 4, 1979
ReceivedNov 19, 1979
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K792335

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.