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MODIFICATION TO VISITOME 20-10 MICROKERATOME

Biovision AG · Class I · Cleared Nov 16, 2004

K-numberK042083
Device nameMODIFICATION TO VISITOME 20-10 MICROKERATOME
ApplicantBiovision AG
Product codeHNO
Device classClass I
Decision dateNov 16, 2004
DecisionSubstantially Equivalent
Regulation886.4370
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View the full FDA submission: accessdata.fda.gov

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