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

    3RD GENERATION TSH ASSAY FOR THE BAYER IMMUNO 1 SYSTEM

    K Number: K981312 · Decision Jun 5, 1998
    View on FDA
    Classifications
    1
    FEI Numbers
    73
    Registration Numbers
    73
    Same Product Code
    241
    Applicant Total
    96
    Review Days
    56

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    Basic Information

    Device Name
    3RD GENERATION TSH ASSAY FOR THE BAYER IMMUNO 1 SYSTEM
    K Number
    K981312
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    862.1690
    Medical Specialty
    Clinical Chemistry
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Bayer Corp.
    Date Received
    April 10, 1998
    Decision Date
    June 5, 1998
    Product Code
    JLW
    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
    JLW Radioimmunoassay, Thyroid-Stimulating Hormone

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