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

    CHAKOFF ENDOSCOPY

    K Number: K945421 · Decision Dec 23, 1994
    View on FDA
    Classifications
    1
    FEI Numbers
    81
    Registration Numbers
    81
    Same Product Code
    1
    Applicant Total
    16
    Review Days
    49

    Basic Information

    Device Name
    CHAKOFF ENDOSCOPY
    K Number
    K945421
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    876.4530
    Medical Specialty
    Gastroenterology, Urology
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    STEPHEN CHAKOFF, INC.
    Date Received
    November 4, 1994
    Decision Date
    December 23, 1994
    Product Code
    FDG
    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
    FDG Retractor, Fiberoptic

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    Other Clearances by STEPHEN CHAKOFF, INC.

    K Number Device Name
    K940316 HYSTERSCOPE
    K940317 SINUSCOPE
    K950753 CHAKOFF ENDOSCOPY (CAMERA TELEVISION ENDOSCOPIC WITHOUT AUDIO
    K951082 CHAKOFF ENDOSCOPY, RIGID ENDOSCOPE
    K950745 CHAKOFF ENDOSCOPY (ENDOSCOPE AND/OR ACCESSORIES)
    K950748 CHAKOFF ENDOSCOPY (FIBER OPTIC LIGHT SOURCE ROUTINE)
    K950746 CHAKOFF ENDOSCOPY (SET LAPAROSCOPY)
    K950744 CHAKOFF ENDOSCOPY (RIDGID ENDOSCOPE)
    K950747 CHAKOFF ENDOSCOPY (LIGHT SOURCE ENDOSCOPIC XENON ARC.)
    K945420 CHAKOFF ENDOSCOPY
    Search all 16 clearances from STEPHEN CHAKOFF, INC. →