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

    CO2 INSUFFLATION TUBING

    K Number: K922038 · Decision Oct 13, 1992
    View on FDA
    Classifications
    1
    FEI Numbers
    141
    Registration Numbers
    141
    Same Product Code
    176
    Applicant Total
    10
    Review Days
    165

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    Basic Information

    Device Name
    CO2 INSUFFLATION TUBING
    K Number
    K922038
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    884.1730
    Medical Specialty
    Obstetrics/Gynecology
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Surgeon Surgical Instrumentation, Inc.
    Date Received
    May 1, 1992
    Decision Date
    October 13, 1992
    Product Code
    HIF
    Advisory Committee
    Obstetrics/Gynecology
    Review Advisory Committee
    OB
    Third Party
    N

    Classifications

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

    Product Code Device Name
    HIF Insufflator, Laparoscopic

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    K880543 UNI-PORT
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    K861203 MULTI-SPIKE
    K852229 STERILE EYE PACKS OR TRAYS
    K830859 I/A KIT