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ANSELL NO POWDER AMBI PATIENT EXAMINATION GLOVES

Ansell, Inc. · Class I · Cleared Mar 11, 1993

K-numberK913766
Device nameANSELL NO POWDER AMBI PATIENT EXAMINATION GLOVES
ApplicantAnsell, Inc.
Product codeLYY
Device classClass I
Decision dateMar 11, 1993
DecisionSubstantially Equivalent
Regulation880.6250
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