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

    H200 HANNA SUCTION TREPHINE SYSTEM FOR CORNEAL SUR

    K Number: K896473 · Decision Feb 9, 1990
    View on FDA
    Classifications
    1
    FEI Numbers
    26
    Registration Numbers
    26
    Same Product Code
    4
    Applicant Total
    1
    Review Days
    88

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    Basic Information

    Device Name
    H200 HANNA SUCTION TREPHINE SYSTEM FOR CORNEAL SUR
    K Number
    K896473
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    886.4445
    Medical Specialty
    Ophthalmic
    Decision
    Substantially Equivalent
    Applicant
    Emory University School of Medicine
    Date Received
    November 13, 1989
    Decision Date
    February 9, 1990
    Product Code
    HPN
    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
    HPN Magnet, Permanent

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