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

    PERCUTANEOUS RETRACTOR KIT

    K Number: K912903 · Decision Aug 16, 1991
    View on FDA
    Classifications
    1
    FEI Numbers
    548
    Registration Numbers
    548
    Same Product Code
    1422
    Applicant Total
    13
    Review Days
    45

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    Basic Information

    Device Name
    PERCUTANEOUS RETRACTOR KIT
    K Number
    K912903
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    876.1500
    Medical Specialty
    Gastroenterology, Urology
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Applied Urology, Inc.
    Date Received
    July 2, 1991
    Decision Date
    August 16, 1991
    Product Code
    GCJ
    Advisory Committee
    Gastroenterology, Urology
    Review Advisory Committee
    SU
    Third Party
    N

    Classifications

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

    Product Code Device Name
    GCJ Laparoscope, General & Plastic Surgery

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    Other Clearances by Applied Urology, Inc.

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    K912656 ENDOSCOPIC ELECTRODE
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    K903994 URETEROPYELOGRAM CATH FOR RETROGRADE DYE INJECTION
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