BEUDAMED
    FDA 510(k) Substantially Equivalent 🇩🇪 Germany

    UVATEC SUNTAMED 400

    K Number: K828670 · Decision Jan 17, 1983
    View on FDA
    Classifications
    0
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    0
    Applicant Total
    3
    Review Days
    48

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    Basic Information

    Device Name
    UVATEC SUNTAMED 400
    K Number
    K828670
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Applicant
    Solitec GmbH
    Date Received
    November 30, 1982
    Decision Date
    January 17, 1983
    Advisory Committee
    Unknown
    Review Advisory Committee
    RA
    Third Party
    N

    Other Clearances by Solitec GmbH

    K Number Device Name
    K903660 DERMALIGHT PSORACOMB
    K828671 UVATEC SUNTAMED 4000 AND 2000