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VISTITOME 20-10 MICROKERATOME

Biovision AG · Class I · Cleared Mar 11, 2002

K-numberK014000
Device nameVISTITOME 20-10 MICROKERATOME
ApplicantBiovision AG
Product codeHNO
Device classClass I
Decision dateMar 11, 2002
DecisionSubstantially Equivalent
Regulation886.4370
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View the full FDA submission: accessdata.fda.gov

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