510(k) K101702

MIDWEST REPROCESSING CENTER REPROCESSED VENODYNE SLEEVES/FOOT CUFFS by Midwest Reprocessing Center, LLC — Product Code JOW

K101702 is an FDA 510(k) premarket notification submitted by Midwest Reprocessing Center, LLC for the device "MIDWEST REPROCESSING CENTER REPROCESSED VENODYNE SLEEVES/FOOT CUFFS". The FDA issued a decision of Substantially Equivalent on August 27, 2010. The device falls under product code JOW (Sleeve, Limb, Compressible), a Class II device regulated under 21 CFR 870.5800. Midwest Reprocessing Center, LLC has at least 3 other 510(k) clearances on record.