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

    RICHARD-ALLAN VESSEL LOOPS

    K Number: K900566 · Decision May 3, 1990
    View on FDA
    Classifications
    1
    FEI Numbers
    231
    Registration Numbers
    231
    Same Product Code
    66
    Applicant Total
    33
    Review Days
    85

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    Basic Information

    Device Name
    RICHARD-ALLAN VESSEL LOOPS
    K Number
    K900566
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    878.4800
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Applicant
    Richard-Allan Medical Ind., Inc.
    Date Received
    February 7, 1990
    Decision Date
    May 3, 1990
    Product Code
    KDC
    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
    KDC Instrument, Surgical, Disposable

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