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

    SONY LASER VIDEODISC RECORDING SYSTEM

    K Number: K921275 · Decision Jun 10, 1992
    View on FDA
    Classifications
    1
    FEI Numbers
    61
    Registration Numbers
    61
    Same Product Code
    54
    Applicant Total
    6
    Review Days
    82

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    Basic Information

    Device Name
    SONY LASER VIDEODISC RECORDING SYSTEM
    K Number
    K921275
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    892.2010
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Sony Medical Systems
    Date Received
    March 20, 1992
    Decision Date
    June 10, 1992
    Product Code
    LMB
    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
    LMB Device, Digital Image Storage, Radiological

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