510(k) K093018

G-PROX ENDOSCOPIC GRASPER, MODEL 205333 by Usgi Medical — Product Code GAT

K093018 is an FDA 510(k) premarket notification submitted by Usgi Medical for the device "G-PROX ENDOSCOPIC GRASPER, MODEL 205333". The FDA issued a decision of Substantially Equivalent on October 7, 2009. The device falls under product code GAT (Suture, Nonabsorbable, Synthetic, Polyethylene), a Class II device regulated under 21 CFR 878.5000. Usgi Medical has at least 10 other 510(k) clearances on record.