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

    F72T12/BL-S/HO UVA SUNLAMP

    K Number: K811585 · Decision Aug 13, 1981
    View on FDA
    Classifications
    1
    FEI Numbers
    25
    Registration Numbers
    25
    Same Product Code
    271
    Applicant Total
    2
    Review Days
    69

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    Basic Information

    Device Name
    F72T12/BL-S/HO UVA SUNLAMP
    K Number
    K811585
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    878.4630
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Applicant
    Westinghouse Electric Corp.
    Date Received
    June 5, 1981
    Decision Date
    August 13, 1981
    Product Code
    FTC
    Advisory Committee
    General, Plastic Surgery
    Review Advisory Committee
    RA
    Third Party
    N

    Classifications

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

    Product Code Device Name
    FTC Light, Ultraviolet, Dermatological

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    Other Clearances by Westinghouse Electric Corp.

    K Number Device Name
    K811586 F72T12/BL-S/SHO-O UVA SUNLAMP