510(k) K811469

MMG URINARY DRAINAGE TUBING by Medical Marketing Group — Product Code KNX

K811469 is an FDA 510(k) premarket notification submitted by Medical Marketing Group for the device "MMG URINARY DRAINAGE TUBING". The FDA issued a decision of Substantially Equivalent on June 12, 1981. The device falls under product code KNX (Collector, Urine, (And Accessories) For Indwelling Catheter), a Class II device regulated under 21 CFR 876.5250. Medical Marketing Group has at least 10 other 510(k) clearances on record.