510(k) K002380

INFUSOR SV, INFUSOR LV, BAXTER PAIN MANAGEMENT SYSTEM by Baxter Healthcare Corp — Product Code FRN

K002380 is an FDA 510(k) premarket notification submitted by Baxter Healthcare Corp for the device "INFUSOR SV, INFUSOR LV, BAXTER PAIN MANAGEMENT SYSTEM". The FDA issued a decision of Substantially Equivalent on Sep 5, 2000. The device falls under product code FRN (Pump, Infusion), a Class II device regulated under 21 CFR 880.5725. Baxter Healthcare Corp has 507 other 510(k) clearances on record.