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

    VARICATH PERIPHERAL INFUSION CATHETER

    K Number: K073400 · Decision Dec 20, 2007
    View on FDA
    Classifications
    1
    FEI Numbers
    147
    Registration Numbers
    147
    Same Product Code
    174
    Applicant Total
    2
    Review Days
    16

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    Basic Information

    Device Name
    VARICATH PERIPHERAL INFUSION CATHETER
    K Number
    K073400
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    870.1210
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Veinrx, Inc.
    Date Received
    December 4, 2007
    Decision Date
    December 20, 2007
    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

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    Other Clearances by Veinrx, Inc.

    K Number Device Name
    K052738 INFUSIONCATH PERIPHERAL INFUSION CATHETER, MODELS VF0012, VF0016, VF0024, VF0028, VF0032, VF0036, VF0040, VF0044