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

    KENSORB

    K Number: K953830 · Decision Oct 3, 1995
    View on FDA
    Classifications
    1
    FEI Numbers
    211
    Registration Numbers
    211
    Same Product Code
    110
    Applicant Total
    6
    Review Days
    48

    Research this 510(k) in seconds

    The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

    Free to try · every answer cites its records

    Ask the Research Assistant See examples

    Basic Information

    Device Name
    KENSORB
    K Number
    K953830
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    878.4450
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Kentron Health Care, Inc.
    Date Received
    August 16, 1995
    Decision Date
    October 3, 1995
    Product Code
    GDY
    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
    GDY Gauze/Sponge, Internal, X-Ray Detectable

    Similar 510(k) Clearances

    Other 510(k) clearances with the same product code (GDY), ordered by most recent decision date.

    ULTRACELL SUCTION SPONGE

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    CPR LAP SPONGES

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    STRYKER FEMORAL CANAL SPONGE & ACETABULUM SPONGE

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    PROTEC X-RAY DETECTABLE GAUZE SPONGE

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    TRIANGULAR SPONGES

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    ROSEBUD DISSECTOR

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery
    View all

    Other Clearances by Kentron Health Care, Inc.

    K Number Device Name
    K030693 KENTEX DISPOSABLE VAGINAL SPECULUM
    K972410 IMPERVIOUS ISOLATION GOWN
    K971917 KENTRON'S ISOLATION GOWN
    K953465 KENTEMP
    K953914 KENTEX