510(k) K871209

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

K871209 is an FDA 510(k) premarket notification submitted by Norfolk Medical Products, Inc. for the device "NORFOLK MEDICAL NORPORT". The FDA issued a decision of Substantially Equivalent on June 24, 1987. 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.