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

    VERISTA IMAGING ISOCAM II GAMMA CAMERA

    K Number: K081757 · Decision Aug 15, 2008
    View on FDA
    Classifications
    1
    FEI Numbers
    21
    Registration Numbers
    21
    Same Product Code
    129
    Applicant Total
    1
    Review Days
    56

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    Basic Information

    Device Name
    VERISTA IMAGING ISOCAM II GAMMA CAMERA
    K Number
    K081757
    Device Class
    FDA class 1
    Clearance Type
    Special
    Regulation Number
    892.1100
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Verista Imaging, Inc.
    Date Received
    June 20, 2008
    Decision Date
    August 15, 2008
    Product Code
    IYX
    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
    IYX Camera, Scintillation (Gamma)

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