510(k) K102385

NORFOLK MEDICAL NORPORT FAMILY OF PORTS by Norfolk Medical Products, Inc. — Product Code LJT

K102385 is an FDA 510(k) premarket notification submitted by Norfolk Medical Products, Inc. for the device "NORFOLK MEDICAL NORPORT FAMILY OF PORTS". The FDA issued a decision of Substantially Equivalent on January 14, 2011. 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.