510(k) K960801

SELECTOR ANGIOGRAPHIC CATHETER (VARIOUS MODELS) by North American Instrument Corp. — Product Code DQO

K960801 is an FDA 510(k) premarket notification submitted by North American Instrument Corp. for the device "SELECTOR ANGIOGRAPHIC CATHETER (VARIOUS MODELS)". The FDA issued a decision of Substantially Equivalent on March 29, 1996. The device falls under product code DQO (Catheter, Intravascular, Diagnostic), a Class II device regulated under 21 CFR 870.1200. North American Instrument Corp. has at least 10 other 510(k) clearances on record.