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

    MUELLER HINTON AGAR PLATES P3318/1&2/P3418/P34181

    K Number: K882351 · Decision Jun 28, 1988
    View on FDA
    Classifications
    1
    FEI Numbers
    10
    Registration Numbers
    10
    Same Product Code
    73
    Applicant Total
    89
    Review Days
    21

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    Basic Information

    Device Name
    MUELLER HINTON AGAR PLATES P3318/1&2/P3418/P34181
    K Number
    K882351
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    866.1700
    Medical Specialty
    Microbiology
    Decision
    Substantially Equivalent
    Applicant
    Lakewood Biochemical Co., Inc.
    Date Received
    June 7, 1988
    Decision Date
    June 28, 1988
    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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