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

    UltraVision 2 Diagnostic Ultrasound System

    K Number: K173265 · Decision Nov 7, 2017
    View on FDA
    Classifications
    1
    FEI Numbers
    220
    Registration Numbers
    220
    Same Product Code
    1171
    Applicant Total
    2
    Review Days
    27

    Research this 510(k) in seconds

    The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

    Free to try · every answer cites its records

    Ask the Research Assistant See examples

    Basic Information

    Device Name
    UltraVision 2 Diagnostic Ultrasound System
    K Number
    K173265
    Device Class
    FDA class 2
    Clearance Type
    Abbreviated
    Regulation Number
    892.1550
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Winprobe Corporation
    Date Received
    October 11, 2017
    Decision Date
    November 7, 2017
    Product Code
    IYN
    Advisory Committee
    Radiology
    Review Advisory Committee
    RA
    Third Party
    Y

    Classifications

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

    Product Code Device Name
    IYN System, Imaging, Pulsed Doppler, Ultrasonic

    Similar 510(k) Clearances

    Other 510(k) clearances with the same product code (IYN), ordered by most recent decision date.

    ACUSON Sequoia Diagnostic Ultrasound System;ACUSON Sequoia Select Diagnostic Ultrasound System;ACUSON Origin Diagnostic Ultrasound System;ACUSON Origin ICE Diagnostic Ultrasound System

    FDA 510(k)
    FDA Class 2 ·Radiology

    ES-Series

    FDA 510(k)
    FDA Class 2 ·Radiology

    EPIQ Series Diagnostic Ultrasound System

    FDA 510(k)
    FDA Class 2 ·Radiology

    EPIQ Series Diagnostic Ultrasound Systems; Affiniti Series Diagnostic Ultrasound Systems

    FDA 510(k)
    FDA Class 2 ·Radiology

    LOGIQ e

    FDA 510(k)
    FDA Class 2 ·Radiology

    SonoPort Series Digital Color Doppler Ultrasound System (SonoPort 1, SonoPort 1 Exp, SonoPort 1 Pro, SonoPort 1 Elite, SonoPort 1 Plus, SonoPort 2, SonoPort 2 Exp, SonoPort 2 Pro, SonoPort 2 Elite, SonoPort 2 Plus, SonoPort 3, SonoPort 3 Exp, SonoPort 3 Pro, SonoPort 3 Elite, SonoPort 3 Plus, SonoPort 4, SonoPort 4 Exp, SonoPort 4 Pro, SonoPort 4 Elite, SonoPort 4 Plus, SonoPort 5, SonoPort 5 Exp, SonoPort 5 Pro, SonoPort 5 Elite, SonoPort 5 Plus, SonoPort 6, SonoPort 6 Exp, SonoPort 6

    FDA 510(k)
    FDA Class 2 ·Radiology
    View all

    Other Clearances by Winprobe Corporation

    K Number Device Name
    K150580 UltraVision 2 Diagnostic Ultrasound System