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

    BITESTICK BLOCK

    K Number: K840789 · Decision Apr 5, 1984
    View on FDA
    Classifications
    1
    FEI Numbers
    15
    Registration Numbers
    15
    Same Product Code
    27
    Applicant Total
    2
    Review Days
    62

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    Basic Information

    Device Name
    BITESTICK BLOCK
    K Number
    K840789
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    882.5070
    Medical Specialty
    Neurology
    Decision
    Substantially Equivalent
    Applicant
    Cherry Plastics, Inc.
    Date Received
    February 3, 1984
    Decision Date
    April 5, 1984
    Product Code
    JXL
    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
    JXL Block, Bite

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    Other Clearances by Cherry Plastics, Inc.

    K Number Device Name
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