ClearanceBrief
510(k) K090336 ยท LZA Polymer Patient Examination Glove

SUNMAX ENTERPRISE SHANGHAI CO. POWDER FREE BLUE NITRILE PATIENT EXAMINATION GLOVE TESTED WITH CHEMOTHERAPY DRUGS

ApplicantSunmax Enterprise Shanghai Co. , Ltd., Great Neck NY, US
DecisionSubstantially Equivalent, Jul 1, 2009
ReceivedFeb 10, 2009
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K090336

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.