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

    BIO-INTERFERENCE BLANKING MATERIAL, AM CAT. #2052

    K Number: K872073 · Decision Sep 11, 1987
    View on FDA
    Classifications
    1
    FEI Numbers
    126
    Registration Numbers
    126
    Same Product Code
    244
    Applicant Total
    73
    Review Days
    105

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    Basic Information

    Device Name
    BIO-INTERFERENCE BLANKING MATERIAL, AM CAT. #2052
    K Number
    K872073
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    862.1150
    Medical Specialty
    Clinical Chemistry
    Decision
    Substantially Equivalent
    Applicant
    American Monitor Corp.
    Date Received
    May 29, 1987
    Decision Date
    September 11, 1987
    Product Code
    JIT
    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
    JIT Calibrator, Secondary

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    K892002 NEOCHROME(R) III GLUCOSE
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