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

    CHAKOFF ENDOSCOPY LAPAROSCOPIC INSTRUMENTATION

    K Number: K932632 · Decision Jun 21, 1994
    View on FDA
    Classifications
    1
    FEI Numbers
    823
    Registration Numbers
    823
    Same Product Code
    2306
    Applicant Total
    16
    Review Days
    385

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    Basic Information

    Device Name
    CHAKOFF ENDOSCOPY LAPAROSCOPIC INSTRUMENTATION
    K Number
    K932632
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    878.4400
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Stephen Chakoff, Inc.
    Date Received
    June 1, 1993
    Decision Date
    June 21, 1994
    Product Code
    GEI
    Advisory Committee
    General, Plastic Surgery
    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
    GEI Electrosurgical, Cutting & Coagulation & Accessories

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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
    K950744 CHAKOFF ENDOSCOPY (RIDGID ENDOSCOPE)
    K950745 CHAKOFF ENDOSCOPY (ENDOSCOPE AND/OR ACCESSORIES)
    K950747 CHAKOFF ENDOSCOPY (LIGHT SOURCE ENDOSCOPIC XENON ARC.)
    K950746 CHAKOFF ENDOSCOPY (SET LAPAROSCOPY)
    K950748 CHAKOFF ENDOSCOPY (FIBER OPTIC LIGHT SOURCE ROUTINE)
    K945421 CHAKOFF ENDOSCOPY
    Search all 16 clearances from Stephen Chakoff, Inc. →