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

    MODEL 800-A VERI/PPR

    K Number: K840099 · Decision Nov 28, 1984
    View on FDA
    Classifications
    1
    FEI Numbers
    184
    Registration Numbers
    184
    Same Product Code
    605
    Applicant Total
    10
    Review Days
    323

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    Basic Information

    Device Name
    MODEL 800-A VERI/PPR
    K Number
    K840099
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    882.5890
    Medical Specialty
    Neurology
    Decision
    Substantially Equivalent
    Applicant
    Verite
    Date Received
    January 10, 1984
    Decision Date
    November 28, 1984
    Product Code
    GZJ
    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
    GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief

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    Other Clearances by Verite

    K Number Device Name
    K844727 MODEL 1000
    K840098 MODEL 811 VERI/TENS & PO
    K822929 VERIL/PPR PERSONAL PAIN RELIEVER #800
    K820651 MODEL 860-1 VERI/PROBE
    K813108 MODEL 500 VERI/500
    K813515 VERI/DFS TM #817
    K811351 VERI-FIER
    K810496 VERI/PMS MODEL 815
    K791187 MODEL 810 VERI/TGS