ClearanceBrief
510(k) K844836 ยท GWD Indirect Fluorescent Antibody Test, Entamoeba Histolytica & Rel Sp

HEMOCLIP X-20 AUTOMATIC HEMOCLIP LIGATING APPLIER

ApplicantEdward Weck, Inc., Research Triangle Pa NC, US
DecisionSubstantially Equivalent, Jan 23, 1985
ReceivedDec 12, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K844836

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.