510(k) K863723

NORFOLK NORPORT/SUBCUTAN. IMPLANTED DRUG DEPOT by Norfolk Medical Products, Inc. — Product Code LJT

K863723 is an FDA 510(k) premarket notification submitted by Norfolk Medical Products, Inc. for the device "NORFOLK NORPORT/SUBCUTAN. IMPLANTED DRUG DEPOT". The FDA issued a decision of Substantially Equivalent on October 29, 1986. The device falls under product code LJT (Port & Catheter, Implanted, Subcutaneous, Intravascular), a Class II device regulated under 21 CFR 880.5965. Norfolk Medical Products, Inc. has at least 10 other 510(k) clearances on record.