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510(k) Data Aggregation

    K Number
    K080382
    Device Name
    SELLAS
    Manufacturer
    Date Cleared
    2008-09-24

    (224 days)

    Product Code
    Regulation Number
    878.4810
    Why did this record match?
    Applicant Name (Manufacturer) :

    DINONA CO., LTD.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
    Intended Use
    The SellaS® is intended for use in : Dermatological procedures requiring the coagulation of soft tissue;
    Device Description
    Not Found
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