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

    THERMOMETER, SURVALENT-ELECTRONIC

    K Number: K760421 · Decision Aug 23, 1976
    View on FDA
    Classifications
    1
    FEI Numbers
    488
    Registration Numbers
    488
    Same Product Code
    797
    Applicant Total
    5
    Review Days
    13

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    Basic Information

    Device Name
    THERMOMETER, SURVALENT-ELECTRONIC
    K Number
    K760421
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.2910
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    Arbrook Mfg. Corp.
    Date Received
    August 10, 1976
    Decision Date
    August 23, 1976
    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 Arbrook Mfg. Corp.

    K Number Device Name
    K792016 DISCARD-A-PAD 40-COUNT SHARPS DISPOSAL
    K781847 LATEX, IN-HOUSE COMPOUNDED
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    K770056 GLOVES, SURGEONS,MICRO-TOUCH POWDERFREE