ClearanceBrief
510(k) K013793 ยท LYY Latex Patient Examination Glove

POWDER FREE LATEX EXAMINATION GLOVES WITH ALOE VERA @PH 5.5 AND PROTEIN LABELING CLAIMS

ApplicantShen Wei (Usa), Inc., Union City CA, US
DecisionSubstantially Equivalent, Jan 22, 2002
ReceivedNov 14, 2001
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K013793

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.