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

    VASOBand Vascular Compression Device

    K Number: K203803 · Decision Jan 26, 2021
    View on FDA
    Classifications
    1
    FEI Numbers
    186
    Registration Numbers
    186
    Same Product Code
    203
    Applicant Total
    2
    Review Days
    29

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    Basic Information

    Device Name
    VASOBand Vascular Compression Device
    K Number
    K203803
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.4450
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Vasoinnovations, Inc.
    Date Received
    December 28, 2020
    Decision Date
    January 26, 2021
    Product Code
    DXC
    Advisory Committee
    Cardiovascular
    Review Advisory Committee
    CV
    Third Party
    Y

    Classifications

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

    Product Code Device Name
    DXC Clamp, Vascular

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    Other Clearances by Vasoinnovations, Inc.

    K Number Device Name
    K190318 VASOBand Vascular Compression Device