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FDA 510(k) Applications Submitted by Kaneka Pharma America LLC
FDA 510(k) Number
Submission Date
Device Name
Applicant
K121301
05/01/2012
XPRESSWAY RX CATHETER (6F LD-VERISON)
KANEKA PHARMA AMERICA LLC
K192068
08/01/2019
i-ED COIL
Kaneka Pharma America LLC
K170247
01/27/2017
Lacriflow CL
KANEKA PHARMA AMERICA LLC
K101839
07/01/2010
KANEKA PHARMA AMERICA XPRESS-WAY RX
KANEKA PHARMA AMERICA LLC
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