510(k) K893716

VOLUMETRIC PUMP SOLUTION SET FOR FLO-GARD 8000 by Baxter Healthcare Corp — Product Code FPA

K893716 is an FDA 510(k) premarket notification submitted by Baxter Healthcare Corp for the device "VOLUMETRIC PUMP SOLUTION SET FOR FLO-GARD 8000". The FDA issued a decision of Substantially Equivalent on Sep 18, 1989. The device falls under product code FPA (Set, Administration, Intravascular), a Class II device regulated under 21 CFR 880.5440. Baxter Healthcare Corp has 507 other 510(k) clearances on record.