510(k) Report

510(k) · Cleared

Cleared

UltraVision 2 Diagnostic Ultrasound System

K173265510(k) AbbreviatedCleared Nov 7, 201727-day reviewClass II21 CFR 892.1550

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Winprobe Corporation · IYN System, Imaging, Pulsed Doppler, Ultrasonic

Cleared on Nov 7, 2017 as substantially equivalent to K142876 (Siemens Medical Solutions USA, Inc., 2014) after a 27-day review. Its family tree reaches back 20 generations to 1995. 2 later devices descend from it.

Decided
Nov 7, 2017
Review
27 days
Class
Class II
Product code
IYN
Recalls
None
Predicates
1

Its longest line of descent runs back 20 generations to K935595 (1995). 177 ancestors in all, the oldest K863700 (1987). 2 later devices descend from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2012: 6 other ancestors2011: 3 other ancestors2010: 8 other ancestors2013: 2 other ancestors2009: 8 other ancestors2008: 9 other ancestors2007: 9 other ancestors2006: 8 other ancestors2002: 12 other ancestors2005: 12 other ancestors2004: 16 other ancestors2003: 13 other ancestors2001: 9 other ancestors1998: 3 other ancestors1996: 2 other ancestors2000: 7 other ancestors1997: 6 other ancestors1995: 6 other ancestors1993: 1 other ancestor1988: 1 other ancestor1987: 1 other ancestor1999: 7 other ancestors1992: 1 other ancestor1994: 5 other ancestors1991: 1 other ancestor1989: 1 other ancestor2019: 1 descendant cleared2025: 1 descendant clearedReference device: K150580 · UltraVision 2 Diagnostic Ultrasound System · Winprobe Corporation · 2015K935595 · Acuson Model 3001 · Acuson Corp. · 1995K973767 · Harmonic Imaging with Contrast · Acuson Corp. · 1997K022567 · Sequoia Signature II Diagnostic Ultrasound System · Acuson Corp. · 2002K032114 · Sequoia 8.0 Diagnostic Ultrasound System · Siemens Medical Solutions USA, Inc. · 2003×3: 3 generations cleared close together, K041319 (2004), K042770 (2004), K050240 (2005) K052894 · Sonoline G60 S Ultrasound System · Siemens Medical Solutions USA, Inc. · 2005 · recalled×2: 2 generations cleared close together, K063138 (2006), K063803 (2007) K072786 · Acuson S2000 Ultrasound System · Siemens Medical Solutions USA, Inc. · 2007K083095 · Sonixtouch Ultrasound System · Ultrasonix Medical Corporation · 2008K092271 · GE Logiq E9 BT2010 Diagnostic Ultrasound System, Model 5205000-3, 5205000-4 · GE Healthcare · 2009 · recalledK110943 · Logiq E9 · GE Healthcare · 2011 · recalledK113690 · GE Logiq I, Logiq E and Vivid E · GE Healthcare · 2011 · recalled×2: 2 generations cleared close together, K121699 (2012), K123001 (2012) K132804 · Acuson S1000 / S2000 / S3000 · Siemens Medical Solutions USA, Inc. Ultrasound Gro · 2013 · recalledK140959 · Acuson S1000, S2000, S3000 Diagnostic Ultrasound Systems · Siemens Medical Solutions USA, Inc. · 2014K142876 · ACUSON S1000/ S2000/ S3000 Diagnostic Ultrasound Systems · Siemens Medical Solutions USA, Inc. · 2014 · recalled1990200020102020
Other ancestors, by generationDescendants, by generation 3 generations back: 3 other ancestors4 generations back: 17 other ancestors5 generations back: 35 other ancestors6 generations back: 41 other ancestors7 generations back: 31 other ancestors8 generations back: 13 other ancestors9 generations back: 10 other ancestors10 generations back: 7 other ancestors 1 generation forward: 1 descendant2 generations forward: 1 descendant K142876 · ACUSON S1000/ S2000/ S3000 Diagnostic Ultrasound Systems · Siemens Medical Solutions USA, Inc. · 2014 · recalledK140959 · Acuson S1000, S2000, S3000 Diagnostic Ultrasound Systems · Siemens Medical Solutions USA, Inc. · 2014K132804 · Acuson S1000 / S2000 / S3000 · Siemens Medical Solutions USA, Inc. Ultrasound Gro · 2013 · recalledK123001 · Acuson X700 Diagnstic Ultrasound System · Siemens Medical Solutions USA, Inc. · 2012 · recalledK121699 · Acuson X300 Diagnostic Ultrasound System Sonovista X300 Diagnostic Ultrasound System · Siemens Medical Solutions USA, Inc. · 2012K113690 · GE Logiq I, Logiq E and Vivid E · GE Healthcare · 2011 · recalledK110943 · Logiq E9 · GE Healthcare · 2011 · recalledK092271 · GE Logiq E9 BT2010 Diagnostic Ultrasound System, Model 5205000-3, 5205000-4 · GE Healthcare · 2009 · recalledK083095 · Sonixtouch Ultrasound System · Ultrasonix Medical Corporation · 2008K072786 · Acuson S2000 Ultrasound System · Siemens Medical Solutions USA, Inc. · 2007K063803 · Acuson Antares Diagnostic Ultrasound System · Siemens Medical Solutions USA, Inc., Ultrasound DI · 2007 · recalledK063138 · Modification to Acuson Antares Ultrasound System · Siemens Medical Solutions USA, Inc. · 2006K052894 · Sonoline G60 S Ultrasound System · Siemens Medical Solutions USA, Inc. · 2005 · recalledK050240 · Modification to Acuson CV70 Cardiovascular System · Siemens Medical Solutions USA, Inc. · 2005 · recalledK042770 · Modification to Acuson CV70 Cardiovascular System · Siemens Medical Solutions USA, Inc. · 2004 · recalledK041319 · Sequoia Diagnostic Ultrasound System · Siemens Medical Solutions USA, Inc. · 2004K032114 · Sequoia 8.0 Diagnostic Ultrasound System · Siemens Medical Solutions USA, Inc. · 2003K022567 · Sequoia Signature II Diagnostic Ultrasound System · Acuson Corp. · 2002K973767 · Harmonic Imaging with Contrast · Acuson Corp. · 1997K935595 · Acuson Model 3001 · Acuson Corp. · 1995−20−15−10−50
  1. Root · 20 generations backK935595 Acuson Model 3001Acuson Corp. · 1995
  2. 16 generations between
  3. 3 generations backK132804 Acuson S1000 / S2000 / S3000Siemens Medical Solutions USA, Inc. Ultrasound Gro · 2013 · Recalled
  4. 2 generations backK140959 Acuson S1000, S2000, S3000 Diagnostic Ultrasound SystemsSiemens Medical Solutions USA, Inc. · 2014
  5. 1 generation backK142876 ACUSON S1000/ S2000/ S3000 Diagnostic Ultrasound SystemsSiemens Medical Solutions USA, Inc. · 2014 · Recalled
  6. This deviceK173265 UltraVision 2 Diagnostic Ultrasound SystemWinprobe Corporation · 2017
  7. Descendant · cites it directly · 1 of its ownK190039 EchoSure Diagnostic Ultrasound SystemSonavex, Inc. · 2019
  8. Descendant · 2 generations on · 0 of its ownK243479 EchoGuide (Version 1)Sonavex, Inc. · 2025
Show all 20 generations
  1. Root · 20 generations backK935595 Acuson Model 3001Acuson Corp. · 1995
  2. 19 generations backK973767 Harmonic Imaging with ContrastAcuson Corp. · 1997
  3. 18 generations backK022567 Sequoia Signature II Diagnostic Ultrasound SystemAcuson Corp. · 2002
  4. 17 generations backK032114 Sequoia 8.0 Diagnostic Ultrasound SystemSiemens Medical Solutions USA, Inc. · 2003
  5. 16 generations backK041319 Sequoia Diagnostic Ultrasound SystemSiemens Medical Solutions USA, Inc. · 2004
  6. 15 generations backK042770 Modification to Acuson CV70 Cardiovascular SystemSiemens Medical Solutions USA, Inc. · 2004 · Recalled
  7. 14 generations backK050240 Modification to Acuson CV70 Cardiovascular SystemSiemens Medical Solutions USA, Inc. · 2005 · Recalled
  8. 13 generations backK052894 Sonoline G60 S Ultrasound SystemSiemens Medical Solutions USA, Inc. · 2005 · Recalled
  9. 12 generations backK063138 Modification to Acuson Antares Ultrasound SystemSiemens Medical Solutions USA, Inc. · 2006
  10. 11 generations backK063803 Acuson Antares Diagnostic Ultrasound SystemSiemens Medical Solutions USA, Inc., Ultrasound DI · 2007 · Recalled
  11. 10 generations backK072786 Acuson S2000 Ultrasound SystemSiemens Medical Solutions USA, Inc. · 2007
  12. 9 generations backK083095 Sonixtouch Ultrasound SystemUltrasonix Medical Corporation · 2008
  13. 8 generations backK092271 GE Logiq E9 BT2010 Diagnostic Ultrasound System, Model 5205000-3…GE Healthcare · 2009 · Recalled
  14. 7 generations backK110943 Logiq E9GE Healthcare · 2011 · Recalled
  15. 6 generations backK113690 GE Logiq I, Logiq E and Vivid EGE Healthcare · 2011 · Recalled
  16. 5 generations backK121699 Acuson X300 Diagnostic Ultrasound System Sonovista X300 Diagnostic…Siemens Medical Solutions USA, Inc. · 2012
  17. 4 generations backK123001 Acuson X700 Diagnstic Ultrasound SystemSiemens Medical Solutions USA, Inc. · 2012 · Recalled
  18. 3 generations backK132804 Acuson S1000 / S2000 / S3000Siemens Medical Solutions USA, Inc. Ultrasound Gro · 2013 · Recalled
  19. 2 generations backK140959 Acuson S1000, S2000, S3000 Diagnostic Ultrasound SystemsSiemens Medical Solutions USA, Inc. · 2014
  20. 1 generation backK142876 ACUSON S1000/ S2000/ S3000 Diagnostic Ultrasound SystemsSiemens Medical Solutions USA, Inc. · 2014 · Recalled
  21. This deviceK173265 UltraVision 2 Diagnostic Ultrasound SystemWinprobe Corporation · 2017

Most influential descendants

Showing 2 of 2 · See all
  • K190039EchoSure Diagnostic Ultrasound SystemSonavex, Inc. · 2019 · cites it directly1descendant
  • K243479EchoGuide (Version 1)Sonavex, Inc. · 2025 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−20K935595Acuson Model 3001Acuson Corp.1995—
−19K973767Harmonic Imaging with ContrastAcuson Corp.1997—
−18K022567Sequoia Signature II Diagnostic Ultrasound SystemAcuson Corp.2002—
−17K032114Sequoia 8.0 Diagnostic Ultrasound SystemSiemens Medical Solutions USA, Inc.2003—
−16K041319Sequoia Diagnostic Ultrasound SystemSiemens Medical Solutions USA, Inc.2004—
−15K042770Modification to Acuson CV70 Cardiovascular SystemSiemens Medical Solutions USA, Inc.20041
−14K050240Modification to Acuson CV70 Cardiovascular SystemSiemens Medical Solutions USA, Inc.20051
−13K052894Sonoline G60 S Ultrasound SystemSiemens Medical Solutions USA, Inc.20051
−12K063138Modification to Acuson Antares Ultrasound SystemSiemens Medical Solutions USA, Inc.2006—
−11K063803Acuson Antares Diagnostic Ultrasound SystemSiemens Medical Solutions USA, Inc., Ultrasound DI20079
−10K072786Acuson S2000 Ultrasound SystemSiemens Medical Solutions USA, Inc.2007—
−9K083095Sonixtouch Ultrasound SystemUltrasonix Medical Corporation2008—
−8K092271GE Logiq E9 BT2010 Diagnostic Ultrasound System, Model 5205000-3, 5205000-4GE Healthcare20091
−7K110943Logiq E9GE Healthcare20112
−6K113690GE Logiq I, Logiq E and Vivid EGE Healthcare20111
−5K121699Acuson X300 Diagnostic Ultrasound System Sonovista X300 Diagnostic Ultrasound…Siemens Medical Solutions USA, Inc.2012—
−4K123001Acuson X700 Diagnstic Ultrasound SystemSiemens Medical Solutions USA, Inc.20122
−3K132804Acuson S1000 / S2000 / S3000Siemens Medical Solutions USA, Inc. Ultrasound Gro20133
−2K140959Acuson S1000, S2000, S3000 Diagnostic Ultrasound SystemsSiemens Medical Solutions USA, Inc.2014—
−1K142876ACUSON S1000/ S2000/ S3000 Diagnostic Ultrasound SystemsSiemens Medical Solutions USA, Inc.20141
0 (this device)K173265UltraVision 2 Diagnostic Ultrasound SystemWinprobe Corporation2017—
+1K190039EchoSure Diagnostic Ultrasound SystemSonavex, Inc.2019—
+2K243479EchoGuide (Version 1)Sonavex, Inc.2025—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198710
198810
198910
199110
199210
199310
199450
199560
199620
199760
199830
199970
200070
200190
2002120
2003130
2004160
2005120
200680
200790
200890
200980
201080
201130
201260
201320

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201910
202510
FIG. 1 — Lineage of K173265, 1995–2025Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in IYN? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new IYN device

  1. #1 K240850 EPIQ Series Diagnostic Ultrasound Systems…score 32.1 · 24 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) Report

What was it cleared against? (1)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.

TypeNumberDeviceApplicantDecidedRecalls
*K142876ACUSON S1000/ S2000/ S3000 Diagnostic Ultrasound Systems
Summary page 8
…pler Imaging System 892.1550 IYN Predicate Device: Siemens Acuson S2000 Ultrasound System, K142876 Device Description: The UltraVision 2 is a portable Diagnostic Ultrasound System which applies the latest technologies to produce…
Siemens Medical Solutions USA, Inc.20141
†K150580UltraVision 2 Diagnostic Ultrasound SystemWinprobe Corporation2015—

Also cleared against K142876: 1 other device →

What descends from it? (2)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K190039EchoSure Diagnostic Ultrasound SystemSonavex, Inc.20191

Has anything in its family been recalled? (0 Class I)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • The line of descent spans 22 years and passes through 7 companies; a new generation was cleared every 11 months on median.
  • 47 of the 177 ancestors have a recall of any class.
  • Of its descendants, K190039 (Sonavex, Inc., 2019) has gone furthest, with 1 descendant of its own.
  • 1 other device also cites its predicate K142876.

How does its category compare?

All IYN devices

IYN System, Imaging, Pulsed Doppler, Ultrasonic: FDA decisions, review times, recalls and adverse event reports over 20 years. 2017, this device’s year, is highlighted.

FDA decisions per year · IYN

57in 2025

2007: 132008: 252009: 182010: 292011: 392012: 432013: 512014: 562015: 542016: 602017: 642018: 592019: 472020: 572021: 462022: 532023: 442024: 502025: 572026 (partial year): 44
2007high 64 (2017) · low 13 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · IYN

124in 2025

2007: 26 days median2008: 18 days median2009: 29 days median2010: 67 days median2011: 46 days median2012: 37 days median2013: 60 days median2014: 39 days median2015: 55 days median2016: 56 days median2017: 83 days median2018: 85 days median2019: 79 days median2020: 72 days median2021: 105 days median2022: 105 days median2023: 115 days median2024: 119 days median2025: 124 days median2026 (partial year): 107 days median
2007high 124 (2025) · low 18 (2008)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · IYN

10in 2025

2007: 162008: 122009: 82010: 102011: 82012: 32013: 82014: 22015: 32016: 22018: 72020: 42021: 82022: 102023: 42024: 12025: 102026 (partial year): 2, 1 Class I
2007high 16 (2007) · low 0 (2017)2026

Class I (1 since 2007) Class II/III not classified

Adverse event reports per year · IYN

610in 2025

2007: 32008: 22009: 92010: 172011: 182012: 202013: 182014: 482015: 1162016: 1452017: 1462018: 852019: 592020: 672021: 2132022: 1862023: 2292024: 2662025: 610
2007high 610 (2025) · low 2 (2008)2025

MAUDE reports naming product code IYN, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20071326163
20082518122
2009182989
201029671017
20113946818
20124337320
20135160818
20145639248
201554553116
201660562145
201764830146
20185985785
20194779059
20205772467
2021461058213
20225310510186
2023441154229
2024501191266
20255712410610
2026441072 (1)—

What is it indicated for?

This diagnostic ultrasound system (UltraVision) and its transducers are intended for use in clinical examinations to

evaluate differences in the echogenicity of soft tissue of small parts in adult patients, (thyroid, breast, and testicles) and for

peripheral vessel, abdominal, and superficial muscular skeletal diagnosis.

The system is for prescription use only by a trained sonographer under the direction of a qualified physician or directly by a

qualified physician.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K173265: UltraVision 2 Diagnostic Ultrasound System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K173265

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Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026