510(k) K914048

NEEDLE*LOCK(TM) WITH INTERLINK(TM) INJECTION SITE by Baxter Healthcare Corp — Product Code FPA

K914048 is an FDA 510(k) premarket notification submitted by Baxter Healthcare Corp for the device "NEEDLE*LOCK(TM) WITH INTERLINK(TM) INJECTION SITE". The FDA issued a decision of Substantially Equivalent on Nov 27, 1991. 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.