ClearanceBrief
510(k) K911081 ยท LYY Latex Patient Examination Glove

LATEX PATIENT EXAMINATION GLOVES

ApplicantMedical Device Inspection Co., Inc., Great Neck NY, US
DecisionSubstantially Equivalent, Mar 21, 1991
ReceivedMar 11, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K911081

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.