BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

    MUELLER HINTON AGAR

    K Number: K833861 · Decision Dec 8, 1983
    View on FDA
    Classifications
    1
    FEI Numbers
    10
    Registration Numbers
    10
    Same Product Code
    73
    Applicant Total
    2
    Review Days
    31

    Basic Information

    Device Name
    MUELLER HINTON AGAR
    K Number
    K833861
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    866.1700
    Medical Specialty
    Microbiology
    Decision
    Substantially Equivalent
    Applicant
    AMERICAN BIOMEDICAL CORP.
    Date Received
    November 7, 1983
    Decision Date
    December 8, 1983
    Product Code
    JTZ
    Advisory Committee
    Microbiology
    Review Advisory Committee
    MI
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    JTZ Culture Media, Antimicrobial Susceptibility Test, Mueller Hinton Agar/Broth

    Similar 510(k) Clearances

    Other 510(k) clearances with the same product code (JTZ), ordered by most recent decision date.

    MUELLER HINTON AGAR

    FDA 510(k)
    FDA Class 2 ·Microbiology

    MUELLER HINTON II BROTH (CATION-ADJUSTED) WITH LYSED HORSE BLOOD

    FDA 510(k)
    FDA Class 2 ·Microbiology

    MUELLER HINTON AGAR WITH 5% SHEEP BLOOD

    FDA 510(k)
    FDA Class 2 ·Microbiology

    MUELLER HINTON AGAR WITH 2% NACI

    FDA 510(k)
    FDA Class 2 ·Microbiology

    CULTURE MEDIA, ANTIMICROBIAL SUSCEPTIBILITY TEST, MUELLER HINTON AGARS

    FDA 510(k)
    FDA Class 2 ·Microbiology

    MUELLER HINTON AGAR W/OXACILLIN

    FDA 510(k)
    FDA Class 2 ·Microbiology
    View all

    Other Clearances by AMERICAN BIOMEDICAL CORP.

    K Number Device Name
    K833862 THAYER MARTIN AGAR