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

    SURGICAL CURETTE

    K Number: K932493 · Decision Jan 7, 1994
    View on FDA
    Classifications
    1
    FEI Numbers
    228
    Registration Numbers
    228
    Same Product Code
    13
    Applicant Total
    1
    Review Days
    228

    Basic Information

    Device Name
    SURGICAL CURETTE
    K Number
    K932493
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    878.4800
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    WHITNEY PRODUCTS, INC.
    Date Received
    May 24, 1993
    Decision Date
    January 7, 1994
    Product Code
    FZS
    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
    FZS Curette, Surgical, General Use

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