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

    AMES TDA SISOMICIN TEST-CONTROL SERUM

    K Number: K832792 · Decision Sep 29, 1983
    View on FDA
    Classifications
    1
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    18
    Applicant Total
    158
    Review Days
    44

    Basic Information

    Device Name
    AMES TDA SISOMICIN TEST-CONTROL SERUM
    K Number
    K832792
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    862.3450
    Medical Specialty
    Clinical Toxicology
    Decision
    Substantially Equivalent
    Applicant
    MILES LABORATORIES, INC.
    Date Received
    August 16, 1983
    Decision Date
    September 29, 1983
    Product Code
    DJB
    Advisory Committee
    Clinical Toxicology
    Review Advisory Committee
    CH
    Third Party
    N

    Classifications

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

    Product Code Device Name
    DJB Radioimmunoassay, Gentamicin (125-I), Second Antibody Sep.

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