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

    THE CALIFORNIA SPLINT

    K Number: K854752 · Decision Dec 17, 1985
    View on FDA
    Classifications
    1
    FEI Numbers
    172
    Registration Numbers
    172
    Same Product Code
    197
    Applicant Total
    4
    Review Days
    21

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    Basic Information

    Device Name
    THE CALIFORNIA SPLINT
    K Number
    K854752
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.1120
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    Intl. Medication Systems, Ltd.
    Date Received
    November 26, 1985
    Decision Date
    December 17, 1985
    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 Intl. Medication Systems, Ltd.

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