ROCKWELL MEDICALTECHNOLOGIES, INC. CITRAPURE

ROCKWELL MEDICALTECHNOLOGIES, INC. CITRAPURE is an FDA 510(k)-cleared medical device (K062399) manufactured by Rockwell Medical Technologies, Inc.. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 16, 2006. Regulation: 8.