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

    NEITZ HALOGEN OPHTHALMOSCOPE BXA-RP

    K Number: K942714 · Decision Aug 5, 1994
    View on FDA
    Classifications
    1
    FEI Numbers
    53
    Registration Numbers
    53
    Same Product Code
    86
    Applicant Total
    24
    Review Days
    57

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    Basic Information

    Device Name
    NEITZ HALOGEN OPHTHALMOSCOPE BXA-RP
    K Number
    K942714
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    886.1570
    Medical Specialty
    Ophthalmic
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Neitz Instruments Company, Ltd.
    Date Received
    June 9, 1994
    Decision Date
    August 5, 1994
    Product Code
    HLI
    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
    HLI Ophthalmoscope, Ac-Powered

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