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

    CULTURE MEDIUM FOR ANTIMICROBIAL SUSCEP

    K Number: K841834 · Decision May 14, 1984
    View on FDA
    Classifications
    1
    FEI Numbers
    10
    Registration Numbers
    10
    Same Product Code
    73
    Applicant Total
    14
    Review Days
    27

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    Basic Information

    Device Name
    CULTURE MEDIUM FOR ANTIMICROBIAL SUSCEP
    K Number
    K841834
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    866.1700
    Medical Specialty
    Microbiology
    Decision
    Substantially Equivalent
    Applicant
    Microline Scientific
    Date Received
    April 17, 1984
    Decision Date
    May 14, 1984
    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

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    Other Clearances by Microline Scientific

    K Number Device Name
    K841586 CHOCOLATE AGAR
    K841843 DIFFERENTIAL CULTURE MED. LEVINE EMB
    K841844 DIFFERENTIAL CULTURE MEDIUM-BIGGY AGAR
    K841842 DIFFERENTIAL CULTURE MED. MACCONKEY AGAR
    K841845 SELECTIVE CULTURE MED. COLUMBIA CNA
    K841841 DIFFERENTIAL CULTURE MED. MANNITOL SALT
    K841840 SELECTIVE CULTURE MED. PHENYLETHYL ALCO
    K841839 SELECTIVE CULTURE MED. SELECTIVE STREP
    K841837 ENRICHED CULTURE MED. FLUID THIOGLYC0
    K841838 ENRICHED CULTURE MED. TRYPTIC SOY AGAR
    Search all 14 clearances from Microline Scientific →