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FDA 510(k) Applications Submitted by KEOSYS S.A.S.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K070606
03/05/2007
VISIO+CD VIEWER# KPSCDVE01
KEOSYS S.A.S.
K102000
07/15/2010
IMAGYS
KEOSYS S.A.S.
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