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

    MICROSURG CAUTERY

    K Number: K810017 · Decision Jan 5, 1981
    View on FDA
    Classifications
    1
    FEI Numbers
    2
    Registration Numbers
    2
    Same Product Code
    11
    Applicant Total
    13
    Review Days
    —

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    Basic Information

    Device Name
    MICROSURG CAUTERY
    K Number
    K810017
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    886.4115
    Medical Specialty
    Ophthalmic
    Decision
    Unknown
    Applicant
    Medical Products Development, Inc.
    Date Received
    January 5, 1981
    Decision Date
    January 5, 1981
    Product Code
    HQO
    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
    HQO Unit, Cautery, Thermal, Ac-Powered

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    Other Clearances by Medical Products Development, Inc.

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    K810015 MULTIHI-TEMP CAUTERY
    K810014 REPLACABLE BATTERY HI-TEMP CAUTERY
    K802942 HITEMP. TM 2 LOOPTIP CAUTERY
    K810018 SURG-FLEX 5 SURGICAL LIGHT
    K810019 SURG-FLEX 15 SURGICAL LIGHT
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