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

    SUTURE SET OR LACERATION TRAYS (PACKS)

    K Number: K932219 · Decision Jul 9, 1993
    View on FDA
    Classifications
    1
    FEI Numbers
    329
    Registration Numbers
    330
    Same Product Code
    61
    Applicant Total
    29
    Review Days
    63

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    Basic Information

    Device Name
    SUTURE SET OR LACERATION TRAYS (PACKS)
    K Number
    K932219
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    878.4800
    Medical Specialty
    General, Plastic Surgery
    Decision
    Unknown
    Statement or Summary
    Statement
    Applicant
    Associated Medical Products Co.
    Date Received
    May 7, 1993
    Decision Date
    July 9, 1993
    Product Code
    KDD
    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
    KDD Kit, Surgical Instrument, Disposable

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    Other Clearances by Associated Medical Products Co.

    K Number Device Name
    K932221 NEUROLOGICAL OR CRANI TRAYS (PACKS)
    K932216 C-SECTION, LABOR & DELIVERY TRAYS (PACKS)
    K930507 CUSTOM ORTHOPAEDIC TRAYS (PACKS)
    K932217 MAJOR, MINOR, BASIN TRAYS (PACKS)
    K932220 LAP CHOLY TRAYS (PACKS)
    K932218 CARDIAC CATH OR ANGIOGRAPHIC TRAYS
    K842983 AMPCO OPTHALMIC TRAY
    K843114 AMPCO PROCEDURE TRAYS / PACKS
    K823839 AMPCO KIDNEY DIALYSIS TRAY
    K821579 SKIN SCRUB-TRAY
    Search all 29 clearances from Associated Medical Products Co. →