510(k) K903417

VAS-CATH OPTI-PLAST 5F PERIPHERAL ANGIOPLASTY CATH by Vas-Cath, Inc. — Product Code LIT

K903417 is an FDA 510(k) premarket notification submitted by Vas-Cath, Inc. for the device "VAS-CATH OPTI-PLAST 5F PERIPHERAL ANGIOPLASTY CATH". The FDA issued a decision of Substantially Equivalent on December 5, 1990. The device falls under product code LIT (Catheter, Angioplasty, Peripheral, Transluminal), a Class II device regulated under 21 CFR 870.1250. Vas-Cath, Inc. has at least 10 other 510(k) clearances on record.