510(k) K040832

C-PORT ANASTOMOSIS SYSTEM (DEPLOYMENT SYSTEM, CLIP, ACCESSORIES), MODEL FG-000050 by Cardica, Inc. — Product Code FZP

K040832 is an FDA 510(k) premarket notification submitted by Cardica, Inc. for the device "C-PORT ANASTOMOSIS SYSTEM (DEPLOYMENT SYSTEM, CLIP, ACCESSORIES), MODEL FG-000050". The FDA issued a decision of Substantially Equivalent on November 10, 2005. The device falls under product code FZP (Clip, Implantable), a Class II device regulated under 21 CFR 878.4300. Cardica, Inc. has at least 10 other 510(k) clearances on record.