ClearanceBrief
510(k) K993793 ยท LYY Latex Patient Examination Glove

GUTHRIE PRIME PRE-POWDERED PATIENT LATEX EXAMINATION GLOVE

ApplicantGuthrie Medicare Products (Melaka) Sdn Bhd, Great Neck NY, US
DecisionSubstantially Equivalent, Jan 12, 2000
ReceivedNov 9, 1999
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K993793

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.