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
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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