ClearanceBrief
510(k) K900869 ยท LYY Latex Patient Examination Glove

NON-STERILE LATEX PROCEDURE GLOVE

ApplicantSri Johani Sdn. Bhd., Chester NJ, US
DecisionSubstantially Equivalent, Mar 9, 1990
ReceivedFeb 23, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K900869

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.