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

    IMC ENDOSCOPIC INSTRUMENT HOLDER

    K Number: K933371 · Decision Aug 6, 1993
    View on FDA
    Classifications
    1
    FEI Numbers
    1
    Registration Numbers
    1
    Same Product Code
    8
    Applicant Total
    14
    Review Days
    28

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    Basic Information

    Device Name
    IMC ENDOSCOPIC INSTRUMENT HOLDER
    K Number
    K933371
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    876.1500
    Medical Specialty
    Gastroenterology, Urology
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Inman Medical Corp.
    Date Received
    July 9, 1993
    Decision Date
    August 6, 1993
    Product Code
    GCS
    Advisory Committee
    Gastroenterology, Urology
    Review Advisory Committee
    GU
    Third Party
    N

    Classifications

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

    Product Code Device Name
    GCS Endoscope, Battery-Powered And Accessories

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    Other Clearances by Inman Medical Corp.

    K Number Device Name
    K933171 INMAN IRRIGATION TAPERED PROBE
    K933169 INMAN ENDOSCOPIC BLUNT DISSECTOR
    K933094 INSUFFLATOR TUBING KIT W/FILTER
    K933382 IMC CABLE/WIRE COVER
    K933774 IMC SALINE WET DRESSING
    K933305 IMC 5.0MM IRRIGATION/ASPIRATION PROBE
    K933306 IMC 5.0MM IRRIGATION/ASPIRATION PROBE W/HOLES
    K933170 INMAN POOLE TIP SUCTION PROBE W/TUBING KIT
    K932762 10.0MM SUCTION/IRRIGATION PROBE & TUBING KIT
    K921291 INMAN MEDICAL PACKING STRIP
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