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

    THERMOMETER, MERCURY/CLINICAL

    K Number: K901790 · Decision Jul 11, 1990
    View on FDA
    Classifications
    1
    FEI Numbers
    35
    Registration Numbers
    35
    Same Product Code
    32
    Applicant Total
    6
    Review Days
    83

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    Basic Information

    Device Name
    THERMOMETER, MERCURY/CLINICAL
    K Number
    K901790
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.2920
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    Perlink USA, Inc.
    Date Received
    April 19, 1990
    Decision Date
    July 11, 1990
    Product Code
    FLK
    Advisory Committee
    General Hospital
    Review Advisory Committee
    HO
    Third Party
    N

    Classifications

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

    Product Code Device Name
    FLK Thermometer, Clinical Mercury

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