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

    GENERAL PURPOSE TEMPERATURE PROBE, SKIN TEMPERATURE PROBE

    K Number: K121999 · Decision Feb 28, 2013
    View on FDA
    Classifications
    1
    FEI Numbers
    488
    Registration Numbers
    488
    Same Product Code
    797
    Applicant Total
    4
    Review Days
    234

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    Basic Information

    Device Name
    GENERAL PURPOSE TEMPERATURE PROBE, SKIN TEMPERATURE PROBE
    K Number
    K121999
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.2910
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Draeger Medical GmbH
    Date Received
    July 9, 2012
    Decision Date
    February 28, 2013
    Product Code
    FLL
    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
    FLL Continuous Measurement Thermometer

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