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

    AOS UNIVERSAL CONNECTING GUIDE TUBE FOR HIGH DOSE RATE AFTERLOADERS

    K Number: K964910 · Decision Mar 10, 1997
    View on FDA
    Classifications
    1
    FEI Numbers
    46
    Registration Numbers
    46
    Same Product Code
    206
    Applicant Total
    9
    Review Days
    91

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    Basic Information

    Device Name
    AOS UNIVERSAL CONNECTING GUIDE TUBE FOR HIGH DOSE RATE AFTERLOADERS
    K Number
    K964910
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    892.5700
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Alpha-Omega Services, Inc.
    Date Received
    December 9, 1996
    Decision Date
    March 10, 1997
    Product Code
    JAQ
    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
    JAQ System, Applicator, Radionuclide, Remote-Controlled

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    Other Clearances by Alpha-Omega Services, Inc.

    K Number Device Name
    K233628 AOS Interstitial Templates, Needles, and Accessories
    K233626 AOS Marker Seeds (SMG0242-025)
    K102811 AOS ORION IR-192 SOURCE CABLE
    K062824 AOS UNIVERSAL CONECTING GUIDE TUBE
    K062823 AOS INTERSTITIAL TEMPLATES, NEEDLES & ACCESSORIES
    K062826 AOS IMPLANT TUBES, IMPLANT NEEDLES & RETAINING BOTTONS
    K062825 AOS MARKER SEEDS
    K991571 10 CURIE IRDIUM 192, CSN00100-192