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

    A&E MEDICAL ELECTROSURGICAL CONNECTING CORDS

    K Number: K930528 · Decision May 17, 1993
    View on FDA
    Classifications
    1
    FEI Numbers
    823
    Registration Numbers
    823
    Same Product Code
    2306
    Applicant Total
    10
    Review Days
    104

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    Basic Information

    Device Name
    A&E MEDICAL ELECTROSURGICAL CONNECTING CORDS
    K Number
    K930528
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    878.4400
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Alto Development Corp.
    Date Received
    February 2, 1993
    Decision Date
    May 17, 1993
    Product Code
    GEI
    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
    GEI Electrosurgical, Cutting & Coagulation & Accessories

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    K915300 A & EM MEDICAL ELECTROSURGICAL PENCIL/ACCESSORIES
    K884783 RANEY CLIP
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    K831867 PRESSURE MONITORING IV BOTTLE CAP
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