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

    Processor, Cervical Cytology Slide, Automated

    PMA: P950039 · Supplement: S029 · Decision Sep 12, 2014
    View on FDA
    Classifications
    1
    FEI Numbers
    7
    Registration Numbers
    7

    Basic Information

    Device Name
    Processor, Cervical Cytology Slide, Automated
    Trade Name
    THIN PREP PROCESSORS
    PMA Number
    P950039
    Supplement Number
    S029
    Device Class
    FDA Class 3
    Product Code
    MKQ
    Generic Name
    Processor, cervical cytology slide, automated
    Medical Specialty
    Unknown
    Advisory Committee
    Pathology
    Decision
    30-Day Notice Accepted
    Decision Code
    OK30
    Decision Date
    September 12, 2014
    Date Received
    August 15, 2014
    Supplement Type
    30-Day Notice
    Supplement Reason
    Process Change - Manufacturer/Sterilizer/Packager/Supplier
    Expedited Review
    N

    Advisory Committee Statement

    THE FOLLOWING TEN CHANGES: QUALITY CONTROL (QC) INSTRUCTIONS FOR MICROSCOPE SLIDES INK AND CHIP, ADD A NEW FRICTION FEEDER EQUIPMENT, TP-00372 DOCUMENTATION UPDATE, ELECTRICAL SAFETY TESTING, TRANSFER OF LEGACY (LEGACY PMR) DOCUMENTATION INTO AGILE DOCUMENT CONTROL SYSTEM, INSTRUCTION CLARIFICATION REGARDING AIR VENT HOLES DURING MACHINE ASSEMBLY, MECHANICAL DRIVER BOARDS TESTING, PRESERVCYT QC TESTING, CHANGE IN OWNERSHIP OF LCD BOARD MANUFACTURER, AND IMPROVEMENT TO FIXTURES USED IN THE SCREEN PRINTING PROCESS (SQUEEGEE).

    Classifications

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

    Product Code Device Name
    MKQ Processor, Cervical Cytology Slide, Automated