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

    JPI ALUMINUM INTERSPACED X-RAY GRID

    K Number: K926261 · Decision Mar 18, 1993
    View on FDA
    Classifications
    1
    FEI Numbers
    20
    Registration Numbers
    20
    Same Product Code
    14
    Applicant Total
    2
    Review Days
    90

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    Basic Information

    Device Name
    JPI ALUMINUM INTERSPACED X-RAY GRID
    K Number
    K926261
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    892.1910
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Jpi, Inc.
    Date Received
    December 18, 1992
    Decision Date
    March 18, 1993
    Product Code
    IXJ
    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
    IXJ Grid, Radiographic

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    Other Clearances by Jpi, Inc.

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