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

    DISPOSABLE SPECIALITY SPONGES

    K Number: K791870 · Decision Nov 5, 1979
    View on FDA
    Classifications
    1
    FEI Numbers
    274
    Registration Numbers
    274
    Same Product Code
    6
    Applicant Total
    6
    Review Days
    45

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    Basic Information

    Device Name
    DISPOSABLE SPECIALITY SPONGES
    K Number
    K791870
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    878.4800
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Applicant
    Carwild Corp.
    Date Received
    September 21, 1979
    Decision Date
    November 5, 1979
    Product Code
    GDI
    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
    GDI Dissector, Surgical, General & Plastic Surgery

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    Other Clearances by Carwild Corp.

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