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

    BASICS ENDOSCOPY SYSTEM

    K Number: K940911 · Decision May 16, 1994
    View on FDA
    Classifications
    1
    FEI Numbers
    52
    Registration Numbers
    52
    Same Product Code
    45
    Applicant Total
    15
    Review Days
    80

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    Basic Information

    Device Name
    BASICS ENDOSCOPY SYSTEM
    K Number
    K940911
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    876.4300
    Medical Specialty
    Gastroenterology, Urology
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Cox Medical Ent., Inc.
    Date Received
    February 25, 1994
    Decision Date
    May 16, 1994
    Product Code
    KGE
    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
    KGE Forceps, Biopsy, Electric

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    Other Clearances by Cox Medical Ent., Inc.

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    K935250 ACCU-PATH
    K924655 COX DISPOSABLE ENDOSCOPE CLEANING BRUSH(CB-X2)
    K923671 COX DISPOSABLE POLYPECTOMY SNARES
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    K914466 COX DISPOSABLE CYTOLOGY BRUSHES
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