BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇯🇵 Japan

    ANEROID SPHYGMOMANOMETER, DOCTOR TYPE

    K Number: K901506 · Decision May 9, 1990
    View on FDA
    Classifications
    1
    FEI Numbers
    172
    Registration Numbers
    172
    Same Product Code
    197
    Applicant Total
    2
    Review Days
    40

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    Basic Information

    Device Name
    ANEROID SPHYGMOMANOMETER, DOCTOR TYPE
    K Number
    K901506
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.1120
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    Yamasu Co. , Ltd.
    Date Received
    March 30, 1990
    Decision Date
    May 9, 1990
    Product Code
    DXQ
    Advisory Committee
    Cardiovascular
    Review Advisory Committee
    CV
    Third Party
    N

    Classifications

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

    Product Code Device Name
    DXQ Blood Pressure Cuff

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    Other Clearances by Yamasu Co. , Ltd.

    K Number Device Name
    K884420 HOME BLOOD PRESSURE KIT, ANEROID