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

    RETINAL TAAK

    K Number: K901275 · Decision Mar 23, 1990
    View on FDA
    Classifications
    1
    FEI Numbers
    4
    Registration Numbers
    4
    Same Product Code
    2
    Applicant Total
    3
    Review Days
    4

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    Basic Information

    Device Name
    RETINAL TAAK
    K Number
    K901275
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    886.3100
    Medical Specialty
    Ophthalmic
    Decision
    Substantially Equivalent
    Applicant
    Alcon Surgical, Inc.
    Date Received
    March 19, 1990
    Decision Date
    March 23, 1990
    Product Code
    HQW
    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
    HQW Clip, Tantalum, Ophthalmic

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