ClearanceBrief
510(k) K913766 ยท LYY Latex Patient Examination Glove

ANSELL NO POWDER AMBI PATIENT EXAMINATION GLOVES

ApplicantAnsell, Inc., Thailand, TH
DecisionSubstantially Equivalent, Mar 11, 1993
ReceivedAug 22, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K913766

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.