510(k) K934640

HMP DUAL POLYSULFONE PORT by Horizon Medical Products, Inc. — Product Code LJT

K934640 is an FDA 510(k) premarket notification submitted by Horizon Medical Products, Inc. for the device "HMP DUAL POLYSULFONE PORT". The FDA issued a decision of Substantially Equivalent - Kit on Feb 25, 1994. The device falls under product code LJT (Port & Catheter, Implanted, Subcutaneous, Intravascular), a Class II device regulated under 21 CFR 880.5965. Horizon Medical Products, Inc. has 15 other 510(k) clearances on record.