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

    MODIFIED SOYBEAN CASEIN DIGEST BROTH

    K Number: K831671 · Decision Jul 28, 1983
    View on FDA
    Classifications
    1
    FEI Numbers
    69
    Registration Numbers
    69
    Same Product Code
    208
    Applicant Total
    93
    Review Days
    66

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    Basic Information

    Device Name
    MODIFIED SOYBEAN CASEIN DIGEST BROTH
    K Number
    K831671
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    866.2300
    Medical Specialty
    Microbiology
    Decision
    Substantially Equivalent
    Applicant
    Isle Media and Sterile Products, Inc.
    Date Received
    May 23, 1983
    Decision Date
    July 28, 1983
    Product Code
    JSG
    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
    JSG Culture Media, Non-Selective And Non-Differential

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