510(k) K990707

MEDTRONIC 5F & 9F ZUMA GUIDING CATHETERS by Medtronics Interventional Vascular — Product Code DQY

K990707 is an FDA 510(k) premarket notification submitted by Medtronics Interventional Vascular for the device "MEDTRONIC 5F & 9F ZUMA GUIDING CATHETERS". The FDA issued a decision of Substantially Equivalent on March 22, 1999. 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.