510(k) K925362

SUB-Q-SET(R) SUBCUTANEOUS INFUSION SET by Baxter Healthcare Corp — Product Code FPA

K925362 is an FDA 510(k) premarket notification submitted by Baxter Healthcare Corp for the device "SUB-Q-SET(R) SUBCUTANEOUS INFUSION SET". The FDA issued a decision of Substantially Equivalent on Aug 28, 1993. 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.