510(k) K950304

DESERET (R) T-PORT (R) MULTI FLO(TM) AND DESERET (R)PRN ADAPTER by Becton Dickinson Vascular Access, Inc. — Product Code FPA

K950304 is an FDA 510(k) premarket notification submitted by Becton Dickinson Vascular Access, Inc. for the device "DESERET (R) T-PORT (R) MULTI FLO(TM) AND DESERET (R)PRN ADAPTER". The FDA issued a decision of Substantially Equivalent on March 14, 1995. The device falls under product code FPA (Set, Administration, Intravascular), a Class II device regulated under 21 CFR 880.5440. Becton Dickinson Vascular Access, Inc. has at least 10 other 510(k) clearances on record.