ClearanceBrief
510(k) K051913 ยท LYY Latex Patient Examination Glove

POWDERED LATEX PATIENT EXAMINATION GLOVES

ApplicantShinemound Enterprise, Inc., North Billerica MA, US
DecisionSubstantially Equivalent, Sep 30, 2005
ReceivedJul 15, 2005
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K051913

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.