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

    CK-MB METHOD FOR THE TECHNICON IMMUNO 1 SYSTEM IN-VITRO

    K Number: K961412 · Decision Jun 18, 1996
    View on FDA
    Classifications
    1
    FEI Numbers
    11
    Registration Numbers
    11
    Same Product Code
    39
    Applicant Total
    96
    Review Days
    67

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    Basic Information

    Device Name
    CK-MB METHOD FOR THE TECHNICON IMMUNO 1 SYSTEM IN-VITRO
    K Number
    K961412
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    862.1215
    Medical Specialty
    Clinical Chemistry
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Bayer Corp.
    Date Received
    April 12, 1996
    Decision Date
    June 18, 1996
    Product Code
    JHY
    Advisory Committee
    Clinical Chemistry
    Review Advisory Committee
    TX
    Third Party
    N

    Classifications

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

    Product Code Device Name
    JHY Colorimetric Method, Cpk Or Isoenzymes

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