510(k) K031123

CODMAN BACTISEAL BARIUM STRIPED CATHETERS by Codman & Shurtleff, Inc. — Product Code HCA

K031123 is an FDA 510(k) premarket notification submitted by Codman & Shurtleff, Inc. for the device "CODMAN BACTISEAL BARIUM STRIPED CATHETERS". The FDA issued a decision of Substantially Equivalent on May 14, 2003. The device falls under product code HCA (Catheter, Ventricular), a Class II device regulated under 21 CFR 882.4100. Codman & Shurtleff, Inc. has at least 10 other 510(k) clearances on record.