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

    HYDROXYLINE

    K Number: K833640 · Decision Feb 27, 1984
    View on FDA
    Classifications
    1
    FEI Numbers
    46
    Registration Numbers
    46
    Same Product Code
    76
    Applicant Total
    2
    Review Days
    133

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    Basic Information

    Device Name
    HYDROXYLINE
    K Number
    K833640
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    872.3250
    Medical Specialty
    Dental
    Decision
    Substantially Equivalent
    Applicant
    George Taub Products & Fusion Co., Inc.
    Date Received
    October 17, 1983
    Decision Date
    February 27, 1984
    Product Code
    EJK
    Advisory Committee
    Dental
    Review Advisory Committee
    DE
    Third Party
    N

    Classifications

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

    Product Code Device Name
    EJK Liner, Cavity, Calcium Hydroxide

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    Other Clearances by George Taub Products & Fusion Co., Inc.

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