ClearanceBrief
510(k) K960386 ยท LYY Latex Patient Examination Glove

HANDSAFE

ApplicantHandsafe Products Sdn. Bhd., Muar, Johor, MY
DecisionSubstantially Equivalent, Jun 21, 1996
ReceivedJan 26, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K960386

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.