BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

    DRIGALSKI LITMUS LACTOSE AGAR

    K Number: K841659 · Decision Jun 7, 1984
    View on FDA
    Classifications
    1
    FEI Numbers
    15
    Registration Numbers
    15
    Same Product Code
    86
    Applicant Total
    93
    Review Days
    45

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    Basic Information

    Device Name
    DRIGALSKI LITMUS LACTOSE AGAR
    K Number
    K841659
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    866.2320
    Medical Specialty
    Microbiology
    Decision
    Substantially Equivalent
    Applicant
    Oxoid U.S.A., Inc.
    Date Received
    April 23, 1984
    Decision Date
    June 7, 1984
    Product Code
    JSF
    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
    JSF Culture Media, Single Biochemical Test

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