BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

    SCIMED(R) VENTURE(TM) II INFUSION CATHETER

    K Number: K945904 · Decision May 19, 1995
    View on FDA
    Classifications
    1
    FEI Numbers
    147
    Registration Numbers
    147
    Same Product Code
    174
    Applicant Total
    8
    Review Days
    168

    Research this 510(k) in seconds

    The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

    Free to try · every answer cites its records

    Ask the Research Assistant See examples

    Basic Information

    Device Name
    SCIMED(R) VENTURE(TM) II INFUSION CATHETER
    K Number
    K945904
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.1210
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Scimed Peripheral Interventions
    Date Received
    December 2, 1994
    Decision Date
    May 19, 1995
    Product Code
    KRA
    Advisory Committee
    Cardiovascular
    Review Advisory Committee
    CV
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    KRA Catheter, Continuous Flush

    Similar 510(k) Clearances

    Other 510(k) clearances with the same product code (KRA), ordered by most recent decision date.

    Verge™ Microcatheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TruSelect™ 2.6 Microcatheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    InVera Infusion Device

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Micro Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    XO Cath Microcatheter (E20-090-S, E20-110-S, E20-130-S, E20-150-S, E20-175-S, E20-220-S, E20-090-B, E20-110-B, E20-130-B, E20-150-B, E20-175-B, E20-220-B, E26-090-S, E26-110-S, E26-130-S, E26-150-S, E26-175-S, E26-220-S, E26-090-B, E26-110-B, E26-130-B, E26-150-B, E26-175-B, E26-220-B,)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Peregrine System Infusion Catheter 4-7 mm, Peregrine System Infusion Catheter 3-4 mm

    FDA 510(k)
    FDA Class 2 ·Cardiovascular
    View all

    Other Clearances by Scimed Peripheral Interventions

    K Number Device Name
    K946272 SCIMED(R) COURIER GUIDE CATHETER
    K944677 SCIMED TRANSENT EX STEERABLE GUIDE WIRE AND ACCESSORIES
    K941710 SCIMED TRANSEND STEERABLE GUIDE WIRE AND ACCESSORIES
    K935501 SCIMED VIPER PTA CATHETER WITH BIOSLIDE HYDROPHILIC COATING
    K934793 SCIMED MAVERICK
    K934359 SCIMED STRIKE STEERABLE GUIDE WIRE
    K934122 SCIMED TRANSEND EX STEERABLE GUIDE WIRE AND ACCESSORIES