FDA 510(k) Applications Submitted by ROB CHIOINI

FDA 510(k) Number Submission Date Device Name Applicant
K062399 08/16/2006 ROCKWELL MEDICALTECHNOLOGIES, INC. CITRAPURE ROCKWELL MEDICAL TECHNOLOGIES, INC.
K160847 03/28/2016 Rockwell Medical CitraPure Acid Concetrate ROCKWELL MEDICAL


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