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UNSTERILE PATIENT EXAMINATION GLOVE

Aladan Corp. · Class I · Cleared Mar 23, 1989

K-numberK890627
Device nameUNSTERILE PATIENT EXAMINATION GLOVE
ApplicantAladan Corp.
Product codeLYY
Device classClass I
Decision dateMar 23, 1989
DecisionSubstantially Equivalent
Regulation880.6250
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View the full FDA submission: accessdata.fda.gov

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