BEUDAMED
    FDA PMA FDA Class 3 Approved 🇺🇸 United States

    Somatic Gene Mutation Detection System

    PMA: P120014 · Supplement: S001 · Decision Jan 30, 2015
    View on FDA
    Classifications
    1
    FEI Numbers
    11
    Registration Numbers
    11

    Basic Information

    Device Name
    Somatic Gene Mutation Detection System
    Trade Name
    THXID-BRAF KIT
    PMA Number
    P120014
    Supplement Number
    S001
    Device Class
    FDA Class 3
    Product Code
    OWD
    Generic Name
    Somatic gene mutation detection system
    Medical Specialty
    Unknown
    Advisory Committee
    Pathology
    Decision
    Approved
    Decision Code
    APPR
    Decision Date
    January 30, 2015
    Date Received
    October 10, 2014
    Supplement Type
    135 Review Track For 30-Day Notice
    Supplement Reason
    Process Change - Manufacturer/Sterilizer/Packager/Supplier
    Expedited Review
    N

    Advisory Committee Statement

    APPROVAL FOR A NEW DETERMINATION METHOD OF PLASMIDS AND TRANSCRIPTS CONCENTRATION DURING THE MANUFACTURING STEP (FGM/POL/ M00454), BY USING NANODROP UV-VIS SPECTROPHOTOMETER TO CHANGE FROM THE OLD METHOD UTILIZING STANDARD UV-VIS SPECTROPHOTOMETER.

    Classifications

    This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    OWD Somatic Gene Mutation Detection System