510(k) K893965

PROLONG INTRAVASCULAR CATHETER by Baxter Healthcare Corp — Product Code FOZ

K893965 is an FDA 510(k) premarket notification submitted by Baxter Healthcare Corp for the device "PROLONG INTRAVASCULAR CATHETER". The FDA issued a decision of Substantially Equivalent on Sep 8, 1989. The device falls under product code FOZ (Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days), a Class II device regulated under 21 CFR 880.5200. Baxter Healthcare Corp has 507 other 510(k) clearances on record.