510(k) K932933

GC IV CORONARY GUIDING CATHETER by Medtronics Interventional Vascular — Product Code DQY

K932933 is an FDA 510(k) premarket notification submitted by Medtronics Interventional Vascular for the device "GC IV CORONARY GUIDING CATHETER". The FDA issued a decision of Substantially Equivalent on February 1, 1994. 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.