BEUDAMED
    FDA 510(k) FDA class 2 Unknown 🇺🇸 United States

    ANGIOGRAPHY DRAPE PACK

    K Number: K902293 · Decision Jul 19, 1990
    View on FDA
    Classifications
    1
    FEI Numbers
    159
    Registration Numbers
    159
    Same Product Code
    109
    Applicant Total
    2
    Review Days
    58

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    Basic Information

    Device Name
    ANGIOGRAPHY DRAPE PACK
    K Number
    K902293
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    878.4370
    Medical Specialty
    General, Plastic Surgery
    Decision
    Unknown
    Applicant
    Biocor Medical, Inc.
    Date Received
    May 22, 1990
    Decision Date
    July 19, 1990
    Product Code
    LRO
    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
    LRO General Surgery Tray

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    Other Clearances by Biocor Medical, Inc.

    K Number Device Name
    K910084 SURGICAL DRAPE