510(k) K950179

MEDTRONIC(R) GC III CORONARY GUIDING CATHETER by Medtronics Interventional Vascular — Product Code DQY

K950179 is an FDA 510(k) premarket notification submitted by Medtronics Interventional Vascular for the device "MEDTRONIC(R) GC III CORONARY GUIDING CATHETER". The FDA issued a decision of Substantially Equivalent on July 25, 1995. The device falls under product code DQY (Catheter, Percutaneous), a Class II device regulated under 21 CFR 870.1250. Medtronics Interventional Vascular has at least 10 other 510(k) clearances on record.