BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇳 China

    Electronic Thermometer

    K Number: K152739 · Decision Feb 9, 2016
    View on FDA
    Classifications
    1
    FEI Numbers
    488
    Registration Numbers
    488
    Same Product Code
    797
    Applicant Total
    21
    Review Days
    139

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    Basic Information

    Device Name
    Electronic Thermometer
    K Number
    K152739
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.2910
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Guangdong Biolight Meditech Co., Ltd.
    Date Received
    September 23, 2015
    Decision Date
    February 9, 2016
    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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    Other Clearances by Guangdong Biolight Meditech Co., Ltd.

    K Number Device Name
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    K151287 Fingertip Pulse Oximeters M70, M70A, M70B, M70C, M70D
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    K131762 HANDHELD MONITOR
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