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FDA 510(k) Applications Submitted by BIOVISION AG
FDA 510(k) Number
Submission Date
Device Name
Applicant
K042083
08/03/2004
MODIFICATION TO VISITOME 20-10 MICROKERATOME
BIOVISION AG
K014000
12/04/2001
VISTITOME 20-10 MICROKERATOME
BIOVISION AG
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