BEUDAMED
    FDA PMA FDA Class 2 Approved 🇺🇸 United States

    System, Test, Automated, Antimicrobial Susceptibility, Short Incubation

    PMA: P800029 · Supplement: S005 · Decision Jul 5, 1983
    View on FDA
    Classifications
    1
    FEI Numbers
    23
    Registration Numbers
    23

    Basic Information

    Device Name
    System, Test, Automated, Antimicrobial Susceptibility, Short Incubation
    Trade Name
    OMNISCEPT(TM) KB SYSTEM
    PMA Number
    P800029
    Supplement Number
    S005
    Device Class
    FDA Class 2
    Product Code
    LON
    Generic Name
    SYSTEM, TEST, AUTOMATED, ANTIMICROBIAL SUSCEPTIBILITY, SHORT INCUBATION
    Regulation Number
    866.1645
    Medical Specialty
    Microbiology
    Advisory Committee
    Microbiology
    Decision
    Approved
    Decision Code
    APPR
    Decision Date
    July 5, 1983
    Date Received
    December 3, 1982
    Expedited Review
    N

    Classifications

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

    Product Code Device Name
    LON System, Test, Automated, Antimicrobial Susceptibility, Short Incubation