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

    SURGEONS CHOICE STAPLE, REMOVE/IMPLANT

    K Number: K802783 · Decision Dec 16, 1980
    View on FDA
    Classifications
    1
    FEI Numbers
    8
    Registration Numbers
    8
    Same Product Code
    1
    Applicant Total
    1
    Review Days
    42

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    Basic Information

    Device Name
    SURGEONS CHOICE STAPLE, REMOVE/IMPLANT
    K Number
    K802783
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    878.4200
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Applicant
    Hospital Products Intl.
    Date Received
    November 4, 1980
    Decision Date
    December 16, 1980
    Product Code
    GBN
    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
    GBN Catheter, Pediatric, General & Plastic Surgery

    Similar 510(k) Clearances

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

    MEDDRAINS

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