510(k) K952074

SOLUTION SET WITH 1.2 MICRON AIR ELIMINATING FILTER by Baxter Healthcare Corp — Product Code FPA

K952074 is an FDA 510(k) premarket notification submitted by Baxter Healthcare Corp for the device "SOLUTION SET WITH 1.2 MICRON AIR ELIMINATING FILTER". The FDA issued a decision of Substantially Equivalent on Jul 27, 1995. 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.