510(k) K133264

NMI PICC III by Navilyst Medical, Inc. — Product Code LJS

K133264 is an FDA 510(k) premarket notification submitted by Navilyst Medical, Inc. for the device "NMI PICC III". The FDA issued a decision of Substantially Equivalent on November 20, 2013. The device falls under product code LJS (Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days), a Class II device regulated under 21 CFR 880.5970. Navilyst Medical, Inc. has at least 10 other 510(k) clearances on record.