510(k) K040713

MODIFICATION TO BRAIDED GUIDING INTRODUCER SYSTEM by Thomas Medical Products, Inc. — Product Code DYB

K040713 is an FDA 510(k) premarket notification submitted by Thomas Medical Products, Inc. for the device "MODIFICATION TO BRAIDED GUIDING INTRODUCER SYSTEM". The FDA issued a decision of Substantially Equivalent on June 1, 2004. The device falls under product code DYB (Introducer, Catheter), a Class II device regulated under 21 CFR 870.1340. Thomas Medical Products, Inc. has at least 10 other 510(k) clearances on record.