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

    WEINSTEIN CORNEAL MIRCOAESTHESIOMETER

    K Number: K920271 · Decision Apr 21, 1992
    View on FDA
    Classifications
    1
    FEI Numbers
    5
    Registration Numbers
    5
    Same Product Code
    1
    Applicant Total
    1
    Review Days
    90

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    Basic Information

    Device Name
    WEINSTEIN CORNEAL MIRCOAESTHESIOMETER
    K Number
    K920271
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    886.1040
    Medical Specialty
    Ophthalmic
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Connecticut Bioinstruments, Inc.
    Date Received
    January 22, 1992
    Decision Date
    April 21, 1992
    Product Code
    HJC
    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
    HJC Esthesiometer, Ocular

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