510(k) K844185

MODIFIED C-DAK by Cd Medical, Inc. — Product Code KOC

K844185 is an FDA 510(k) premarket notification submitted by Cd Medical, Inc. for the device "MODIFIED C-DAK". The FDA issued a decision of Substantially Equivalent on January 3, 1985. The device falls under product code KOC (Accessories, Blood Circuit, Hemodialysis), a Class II device regulated under 21 CFR 876.5820. Cd Medical, Inc. has at least 10 other 510(k) clearances on record.