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

    SUTURE REMOVAL KITS STERILE

    K Number: K833688 · Decision May 31, 1984
    View on FDA
    Classifications
    1
    FEI Numbers
    972
    Registration Numbers
    972
    Same Product Code
    186
    Applicant Total
    6
    Review Days
    213

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    Basic Information

    Device Name
    SUTURE REMOVAL KITS STERILE
    K Number
    K833688
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    880.5240
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    Carwild Corp.
    Date Received
    October 31, 1983
    Decision Date
    May 31, 1984
    Product Code
    KGX
    Advisory Committee
    General Hospital
    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
    KGX Tape And Bandage, Adhesive

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    Other Clearances by Carwild Corp.

    K Number Device Name
    K913303 LAP SPONGES, MODIFIED
    K913302 DISPOSABLE SPECIALTY SPONGES (DISSECTORS)/MODIFIED
    K791872 LAP SPONGES
    K791871 NEUROLOGICAL SPONGES (PATTIES)
    K791870 DISPOSABLE SPECIALITY SPONGES