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

    FORCEPS #101 AND #102

    K Number: K790854 · Decision Jun 5, 1979
    View on FDA
    Classifications
    1
    FEI Numbers
    444
    Registration Numbers
    445
    Same Product Code
    103
    Applicant Total
    7
    Review Days
    32

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    Basic Information

    Device Name
    FORCEPS #101 AND #102
    K Number
    K790854
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    878.4800
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Applicant
    C. Intl.
    Date Received
    May 4, 1979
    Decision Date
    June 5, 1979
    Product Code
    GEN
    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
    GEN Forceps, General & Plastic Surgery

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    Other Clearances by C. Intl.

    K Number Device Name
    K792494 CATHETERIZATION FORCEP
    K790855 SURGICAL DRAPE CLIP #201
    K790853 EASY-SPEC
    K790852 VAGI-SPEC
    K790851 VAGI-PRESS #401
    K790856 PROCTOSCOPE #501