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

    UNITED SURGICAL CORP. DIATHERMIC PLUS

    K Number: K870194 · Decision Feb 20, 1987
    View on FDA
    Classifications
    1
    FEI Numbers
    26
    Registration Numbers
    26
    Same Product Code
    10
    Applicant Total
    7
    Review Days
    31

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    Basic Information

    Device Name
    UNITED SURGICAL CORP. DIATHERMIC PLUS
    K Number
    K870194
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    886.4100
    Medical Specialty
    Ophthalmic
    Decision
    Substantially Equivalent
    Applicant
    United Surgical Corp.
    Date Received
    January 20, 1987
    Decision Date
    February 20, 1987
    Product Code
    HQR
    Advisory Committee
    Ophthalmic
    Review Advisory Committee
    OP
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    HQR Apparatus, Cautery, Radiofrequency, Ac-Powered

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