HY-CHLO(TM)WOUND SCRUB

HY-CHLO(TM)WOUND SCRUB is an FDA 510(k)-cleared medical device (K113312) manufactured by Patrin Pharma. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 20, 2012. Regulation: 8.