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

    Avid IF2

    K Number: K183692 · Decision Jun 12, 2019
    View on FDA
    Classifications
    1
    FEI Numbers
    46
    Registration Numbers
    46
    Same Product Code
    72
    Applicant Total
    2
    Review Days
    163

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    Basic Information

    Device Name
    Avid IF2
    K Number
    K183692
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    882.5890
    Medical Specialty
    Neurology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Vision Quest Industries Inc./Dba VQ Orthocare
    Date Received
    December 31, 2018
    Decision Date
    June 12, 2019
    Product Code
    LIH
    Advisory Committee
    Neurology
    Review Advisory Committee
    NE
    Third Party
    N

    Classifications

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

    Product Code Device Name
    LIH Interferential Current Therapy

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    Other Clearances by Vision Quest Industries Inc./Dba VQ Orthocare

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