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

    OPHTHALMIC A/B SCAN SYSTEM, MODEL 835 -- MODIFIED

    K Number: K923348 · Decision Dec 10, 1992
    View on FDA
    Classifications
    1
    FEI Numbers
    398
    Registration Numbers
    399
    Same Product Code
    408
    Applicant Total
    9
    Review Days
    196

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    Basic Information

    Device Name
    OPHTHALMIC A/B SCAN SYSTEM, MODEL 835 -- MODIFIED
    K Number
    K923348
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    892.1570
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Zeiss Humphrey System
    Date Received
    May 28, 1992
    Decision Date
    December 10, 1992
    Product Code
    ITX
    Advisory Committee
    Radiology
    Review Advisory Committee
    RA
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    ITX Transducer, Ultrasonic, Diagnostic

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