510(k) K932847

CORPAK ENTERAL PUMP by Corpak Co. — Product Code FRN

K932847 is an FDA 510(k) premarket notification submitted by Corpak Co. for the device "CORPAK ENTERAL PUMP". The FDA issued a decision of ST on June 17, 1994. The device falls under product code FRN (Pump, Infusion), a Class II device regulated under 21 CFR 880.5725. Corpak Co. has at least 10 other 510(k) clearances on record.