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

    VISUAL SERUM/URINE HCG COMBO KIT

    K Number: K852437 · Decision Jul 12, 1985
    View on FDA
    Classifications
    1
    FEI Numbers
    102
    Registration Numbers
    102
    Same Product Code
    374
    Applicant Total
    4
    Review Days
    32

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    Basic Information

    Device Name
    VISUAL SERUM/URINE HCG COMBO KIT
    K Number
    K852437
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    862.1155
    Medical Specialty
    Clinical Chemistry
    Decision
    Substantially Equivalent
    Applicant
    American Bioclinical, Inc.
    Date Received
    June 10, 1985
    Decision Date
    July 12, 1985
    Product Code
    JHI
    Advisory Committee
    Clinical Chemistry
    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
    JHI Visual, Pregnancy Hcg, Prescription Use

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