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

    SUNBRONZE SB24C/65 ULTRA

    K Number: K896983 · Decision Jan 3, 1990
    View on FDA
    Classifications
    1
    FEI Numbers
    20
    Registration Numbers
    20
    Same Product Code
    80
    Applicant Total
    3
    Review Days
    20

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    Basic Information

    Device Name
    SUNBRONZE SB24C/65 ULTRA
    K Number
    K896983
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    878.4635
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Applicant
    Sunbronze
    Date Received
    December 14, 1989
    Decision Date
    January 3, 1990
    Product Code
    LEJ
    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
    LEJ Booth, Sun Tan

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    Other Clearances by Sunbronze

    K Number Device Name
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