BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

    THERMAJUST CIRCU-TEMP

    K Number: K780543 · Decision May 26, 1978
    View on FDA
    Classifications
    1
    FEI Numbers
    28
    Registration Numbers
    28
    Same Product Code
    7
    Applicant Total
    6
    Review Days
    53

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    Basic Information

    Device Name
    THERMAJUST CIRCU-TEMP
    K Number
    K780543
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    862.2050
    Medical Specialty
    Clinical Chemistry
    Decision
    Substantially Equivalent
    Applicant
    Techhnilab Instruments, Inc.
    Date Received
    April 3, 1978
    Decision Date
    May 26, 1978
    Product Code
    JRQ
    Advisory Committee
    Clinical Chemistry
    Review Advisory Committee
    CH
    Third Party
    N

    Classifications

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

    Product Code Device Name
    JRQ Shaker/Stirrer

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