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

    ARTHOCARE ARTHROSCOPIC ELECTROSURGERY SYSTEM MODEL 970

    K Number: K962321 · Decision Jul 19, 1996
    View on FDA
    Classifications
    1
    FEI Numbers
    386
    Registration Numbers
    386
    Same Product Code
    680
    Applicant Total
    112
    Review Days
    32

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    Basic Information

    Device Name
    ARTHOCARE ARTHROSCOPIC ELECTROSURGERY SYSTEM MODEL 970
    K Number
    K962321
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    888.1100
    Medical Specialty
    Orthopedic
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Arthrocare Corp.
    Date Received
    June 17, 1996
    Decision Date
    July 19, 1996
    Product Code
    HRX
    Advisory Committee
    Orthopedic
    Review Advisory Committee
    OR
    Third Party
    N

    Classifications

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

    Product Code Device Name
    HRX Arthroscope

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