510(k) K020660

HOMEPUMP, ECLIPSE, C-SERIES, PAINBUSTER, C-BLOC, ON-Q, EASYPUMP, ONE STEP KVO by I-Flow Corp. — Product Code MEB

K020660 is an FDA 510(k) premarket notification submitted by I-Flow Corp. for the device "HOMEPUMP, ECLIPSE, C-SERIES, PAINBUSTER, C-BLOC, ON-Q, EASYPUMP, ONE STEP KVO". The FDA issued a decision of Substantially Equivalent on March 20, 2002. The device falls under product code MEB (Pump, Infusion, Elastomeric), a Class II device regulated under 21 CFR 880.5725. I-Flow Corp. has at least 10 other 510(k) clearances on record.