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

    DERMACLEAR UV-B PHOTOTHERAPY SYSTEM

    K Number: K011197 · Decision Dec 14, 2001
    View on FDA
    Classifications
    1
    FEI Numbers
    25
    Registration Numbers
    25
    Same Product Code
    271
    Applicant Total
    5
    Review Days
    239

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    Basic Information

    Device Name
    DERMACLEAR UV-B PHOTOTHERAPY SYSTEM
    K Number
    K011197
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    878.4630
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Lumenis
    Date Received
    April 19, 2001
    Decision Date
    December 14, 2001
    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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