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

    BLACK LAMPS,F72T12/BL/HO

    K Number: K770862 · Decision Jun 27, 1977
    View on FDA
    Classifications
    1
    FEI Numbers
    25
    Registration Numbers
    25
    Same Product Code
    271
    Applicant Total
    5
    Review Days
    48

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    Basic Information

    Device Name
    BLACK LAMPS,F72T12/BL/HO
    K Number
    K770862
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    878.4630
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Applicant
    Dermatron Corp.
    Date Received
    May 10, 1977
    Decision Date
    June 27, 1977
    Product Code
    FTC
    Advisory Committee
    General, Plastic Surgery
    Review Advisory Committee
    SU
    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 Dermatron Corp.

    K Number Device Name
    K761094 UVA PHOTOTHERAPY SYSTEM
    K760471 LAMP, FLOURESCENT BLACK, HIGH OUTPUT
    K760482 SUNLAMP (F40-UVB & F20-UVB)
    K760519 SUNLAMP, FLOURESCENT DERMATRON F40-313 AND F20-313