BEUDAMED
    FDA PMA FDA Class 3 30-Day Notice Accepted 🇺🇸 United States

    Somatic Gene Mutation Detection System

    PMA: P110020 · Supplement: S002 · Decision Oct 26, 2011
    View on FDA
    Classifications
    1
    FEI Numbers
    11
    Registration Numbers
    11

    Basic Information

    Device Name
    Somatic Gene Mutation Detection System
    Trade Name
    COBAS 4800 BRAF V600 MUTATION TEST
    PMA Number
    P110020
    Supplement Number
    S002
    Device Class
    FDA Class 3
    Product Code
    OWD
    Generic Name
    Somatic gene mutation detection system
    Medical Specialty
    Unknown
    Advisory Committee
    Pathology
    Decision
    30-Day Notice Accepted
    Decision Code
    OK30
    Decision Date
    October 26, 2011
    Date Received
    September 29, 2011
    Supplement Type
    30-Day Notice
    Supplement Reason
    Process Change - Manufacturer/Sterilizer/Packager/Supplier
    Expedited Review
    N

    Advisory Committee Statement

    CHANGES TO THE FILLING AND LABELING EQUIPMENT AND LOCATION FOR CERTAIN VIALED INTERMEDIATE COMPONENTS. YOUR FIRM HAS PROPOSED RELOCATION TO BUILDING 502 ROOMS1F24 AND 1F26 FROM BUILDING 502 ROOMS 1F23 AND 1F31 FOR USE OF NEW EQUIPMENT KUGLER LINOLINE 120 FILING AND SCREW-CAPPING LINE WHICH INCLUDES THE ACCRAPLY 4000 AND 35T LABELINGMACHINES.

    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