ClearanceBrief
510(k) K033777 ยท LZA Polymer Patient Examination Glove

ULTRASENSE AF BLUE POWDER-FREE NITRILE EXAMINATION GLOVES

ApplicantSyntex Healthcare Products Co., Ltd., Reno NV, US
DecisionSubstantially Equivalent, Feb 5, 2004
ReceivedDec 4, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K033777

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.