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

    MICROSURGICAL INSTRUMENTS

    K Number: K932169 · Decision Jul 20, 1993
    View on FDA
    Classifications
    1
    FEI Numbers
    136
    Registration Numbers
    136
    Same Product Code
    12
    Applicant Total
    1
    Review Days
    76

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    Basic Information

    Device Name
    MICROSURGICAL INSTRUMENTS
    K Number
    K932169
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    882.4525
    Medical Specialty
    Neurology
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    American Russian Medical Services, Inc.
    Date Received
    May 5, 1993
    Decision Date
    July 20, 1993
    Product Code
    GZX
    Advisory Committee
    Neurology
    Review Advisory Committee
    NE
    Third Party
    N

    Classifications

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

    Product Code Device Name
    GZX Instrument, Microsurgical

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