510(k) Report

510(k) · Cleared

Cleared

S12 Digital Color Doppler Ultrasound System

K142474510(k) TraditionalCleared Dec 19, 2014107-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

Sonoscape Company Limited · IYN System, Imaging, Pulsed Doppler, Ultrasonic

Cleared on Dec 19, 2014 as substantially equivalent to K132768 (Sonoscape Company Limited, 2013) and 1 other predicate after a 107-day review. Its family tree reaches back 16 generations to 1995. 6 of the 133 devices in its family, counting itself, have a Class I recall. 4 later devices descend from it.

Decided
Dec 19, 2014
Review
107 days
Class
Class II
Product code
IYN
Recalls
None
Predicates
2

Its longest line of descent runs back 16 generations to K935595 (1995). 128 ancestors in all, the oldest K882383 (1988). 4 later devices descend from it, 2 citing it directly. 6 of the 133 devices in this family, counting this one, have a Class I recall.

Other ancestors, by year clearedDescendants, by year cleared 2013: 2 other ancestors2012: 1 other ancestor2010: 1 other ancestor2004: 11 other ancestors, 1 with a Class I recall12003: 8 other ancestors2011: 1 other ancestor2006: 2 other ancestors2002: 14 other ancestors2000: 12 other ancestors, 1 with a Class I recall11999: 11 other ancestors1997: 6 other ancestors2005: 6 other ancestors2001: 10 other ancestors1998: 10 other ancestors, 3 with a Class I recall31996: 3 other ancestors, 1 with a Class I recall11995: 5 other ancestors1994: 5 other ancestors1993: 1 other ancestor1988: 1 other ancestor1992: 1 other ancestor1989: 1 other ancestor2017: 2 descendants cleared2015: 1 descendant cleared2022: 1 descendant clearedK935595 · 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. · 2007K091970 · Aixplorer Ultrasound System · Supersonic Imagine · 2009K102041 · Aixplorer · Supersonic Imagine · 2010K112255 · Aixplorer · Supersonic Imagine · 2012×2: 2 generations cleared close together, K130499 (2013), K132304 (2013) 1990200020102020
Other ancestors, by generationDescendants, by generation 1 generation back: 1 other ancestor2 generations back: 5 other ancestors3 generations back: 10 other ancestors4 generations back: 43 other ancestors, 6 with a Class I recall65 generations back: 10 other ancestors6 generations back: 10 other ancestors7 generations back: 7 other ancestors8 generations back: 8 other ancestors9 generations back: 9 other ancestors10 generations back: 9 other ancestors 1 generation forward: 2 descendants2 generations forward: 2 descendants K132304 · Epiq Diagnostic Ultrasound System · Philips Ultrasound, Inc. · 2013 · recalledK130499 · IU22 Diagnostic Ultrasound System · Philips Ultrasound, Inc. · 2013 · recalledK112255 · Aixplorer · Supersonic Imagine · 2012K102041 · Aixplorer · Supersonic Imagine · 2010K091970 · Aixplorer Ultrasound System · Supersonic Imagine · 2009K072786 · 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. · 1995−15−10−50
  1. Root · 16 generations backK935595 Acuson Model 3001Acuson Corp. · 1995
  2. 12 generations between
  3. 3 generations backK112255 AixplorerSupersonic Imagine · 2012
  4. 2 generations backK130499 IU22 Diagnostic Ultrasound SystemPhilips Ultrasound, Inc. · 2013 · Recalled
  5. 1 generation backK132304 Epiq Diagnostic Ultrasound SystemPhilips Ultrasound, Inc. · 2013 · Recalled
  6. This deviceK142474 S12 Digital Color Doppler Ultrasound SystemSonoscape Company Limited · 2014
  7. Descendant · cites it directly · 1 of its ownK171926 C5 Diagnostic Ultrasound SystemGuangzhou Sonostar Technologies Co., Ltd. · 2017
  8. Descendant · cites it directly · 1 of its ownK152396 S12 Digital Color Doppler Ultrasound SystemSonoscape Medical Corp. · 2015
  9. Descendant · 2 generations on · 0 of its ownK220169 SonoMe Wireless Probe Type Ultrasound Scanner (Model: 5C, 5CB, H5C…Bionet Co., Ltd. · 2022
  10. Descendant · 2 generations on · 0 of its ownK170078 Medisono Color Doppler Ultrasound System, models P11 Portable, P11…Medisono, LLC · 2017
Show all 16 generations
  1. Root · 16 generations backK935595 Acuson Model 3001Acuson Corp. · 1995
  2. 15 generations backK973767 Harmonic Imaging with ContrastAcuson Corp. · 1997
  3. 14 generations backK022567 Sequoia Signature II Diagnostic Ultrasound SystemAcuson Corp. · 2002
  4. 13 generations backK032114 Sequoia 8.0 Diagnostic Ultrasound SystemSiemens Medical Solutions USA, Inc. · 2003
  5. 12 generations backK041319 Sequoia Diagnostic Ultrasound SystemSiemens Medical Solutions USA, Inc. · 2004
  6. 11 generations backK042770 Modification to Acuson CV70 Cardiovascular SystemSiemens Medical Solutions USA, Inc. · 2004 · Recalled
  7. 10 generations backK050240 Modification to Acuson CV70 Cardiovascular SystemSiemens Medical Solutions USA, Inc. · 2005 · Recalled
  8. 9 generations backK052894 Sonoline G60 S Ultrasound SystemSiemens Medical Solutions USA, Inc. · 2005 · Recalled
  9. 8 generations backK063138 Modification to Acuson Antares Ultrasound SystemSiemens Medical Solutions USA, Inc. · 2006
  10. 7 generations backK063803 Acuson Antares Diagnostic Ultrasound SystemSiemens Medical Solutions USA, Inc., Ultrasound DI · 2007 · Recalled
  11. 6 generations backK072786 Acuson S2000 Ultrasound SystemSiemens Medical Solutions USA, Inc. · 2007
  12. 5 generations backK091970 Aixplorer Ultrasound SystemSupersonic Imagine · 2009
  13. 4 generations backK102041 AixplorerSupersonic Imagine · 2010
  14. 3 generations backK112255 AixplorerSupersonic Imagine · 2012
  15. 2 generations backK130499 IU22 Diagnostic Ultrasound SystemPhilips Ultrasound, Inc. · 2013 · Recalled
  16. 1 generation backK132304 Epiq Diagnostic Ultrasound SystemPhilips Ultrasound, Inc. · 2013 · Recalled
  17. This deviceK142474 S12 Digital Color Doppler Ultrasound SystemSonoscape Company Limited · 2014

Class I recalls in this family

Most influential descendants

Showing 4 of 4 · See all
  • K171926C5 Diagnostic Ultrasound SystemGuangzhou Sonostar Technologies Co., Ltd. · 2017 · cites it directly1descendant
  • K152396S12 Digital Color Doppler Ultrasound SystemSonoscape Medical Corp. · 2015 · cites it directly1descendant
  • K220169SonoMe Wireless Probe Type Ultrasound Scanner (Model: 5C, 5CB, H5C, 10L, 14L, 10LB…Bionet Co., Ltd. · 2022 · 2 generations on0descendants
  • K170078Medisono Color Doppler Ultrasound System, models P11 Portable, P11 EXPERT Portable, P12…Medisono, LLC · 2017 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−16K935595Acuson Model 3001Acuson Corp.1995—
−15K973767Harmonic Imaging with ContrastAcuson Corp.1997—
−14K022567Sequoia Signature II Diagnostic Ultrasound SystemAcuson Corp.2002—
−13K032114Sequoia 8.0 Diagnostic Ultrasound SystemSiemens Medical Solutions USA, Inc.2003—
−12K041319Sequoia Diagnostic Ultrasound SystemSiemens Medical Solutions USA, Inc.2004—
−11K042770Modification to Acuson CV70 Cardiovascular SystemSiemens Medical Solutions USA, Inc.20041
−10K050240Modification to Acuson CV70 Cardiovascular SystemSiemens Medical Solutions USA, Inc.20051
−9K052894Sonoline G60 S Ultrasound SystemSiemens Medical Solutions USA, Inc.20051
−8K063138Modification to Acuson Antares Ultrasound SystemSiemens Medical Solutions USA, Inc.2006—
−7K063803Acuson Antares Diagnostic Ultrasound SystemSiemens Medical Solutions USA, Inc., Ultrasound DI20079
−6K072786Acuson S2000 Ultrasound SystemSiemens Medical Solutions USA, Inc.2007—
−5K091970Aixplorer Ultrasound SystemSupersonic Imagine2009—
−4K102041AixplorerSupersonic Imagine2010—
−3K112255AixplorerSupersonic Imagine2012—
−2K130499IU22 Diagnostic Ultrasound SystemPhilips Ultrasound, Inc.20132
−1K132304Epiq Diagnostic Ultrasound SystemPhilips Ultrasound, Inc.201336
0 (this device)K142474S12 Digital Color Doppler Ultrasound SystemSonoscape Company Limited2014—
+1K171926C5 Diagnostic Ultrasound SystemGuangzhou Sonostar Technologies Co., Ltd.2017—
+1K152396S12 Digital Color Doppler Ultrasound SystemSonoscape Medical Corp.2015—
+2K220169SonoMe Wireless Probe Type Ultrasound Scanner (Model: 5C, 5CB, H5C, 10L, 14L…Bionet Co., Ltd.2022—
+2K170078Medisono Color Doppler Ultrasound System, models P11 Portable, P11 EXPERT…Medisono, LLC2017—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198810
198910
199210
199310
199450
199550
199631
199760
1998103
1999110
2000121
2001100
2002140
200380
2004111
200560
200620
201010
201110
201210
201320

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201510
201720
202210
FIG. 1 — Lineage of K142474, 1995–2022Source: 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.

6 devices in this family have a Class I recall. 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? (2)

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
*K132768S8 Exp Portable Digital Color Doppler Ultrasound System
Summary page 20
…07.92(a) (3)] The identified predicate devices within this submission are as follows: SonoScape S8 Exp Portable Digital Color Doppler Ultrasound System K132768 Philips EPIQ Diagnostic Ultrasound System K132304 4. Device Description [21 CFR 807.92(a)…
Sonoscape Company Limited2013—
*K132304Epiq Diagnostic Ultrasound System
Summary page 20
…: SonoScape S8 Exp Portable Digital Color Doppler Ultrasound System K132768 Philips EPIQ Diagnostic Ultrasound System K132304 4. Device Description [21 CFR 807.92(a) (4)] This SonoScape S12 Digital Color Doppler Ultrasound System is an integrated…
Philips Ultrasound, Inc.201336

Also cleared against K132768: 4 other devices →

What descends from it? (4)

2 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K171926C5 Diagnostic Ultrasound SystemGuangzhou Sonostar Technologies Co., Ltd.20171
K152396S12 Digital Color Doppler Ultrasound SystemSonoscape Medical Corp.20151

Has anything in its family been recalled? (6 Class I)

No FDA recall names this device.

Relatives with a Class I recall

Class I is FDA’s most serious recall class. A recall in the family tree is context for this device, not evidence about it.

  • K040050Instatrak System with Multiple Dataset Navigation, Model IT3500Ge Medical Systems Navigation and Visualization IN · 2004 · 4 generations back · ◆ in the 2004 ancestors bar of FIG. 11 Class I recall
  • K994270Instatrak 3000 System with Fluorotrak Module, Model IT3000Visualization Technology, Inc. · 2000 · 4 generations back · ◆ in the 2000 ancestors bar of FIG. 12 Class I recalls
  • K983529Instatrak 3000Visualization Technology, Inc. · 1998 · 4 generations back · ◆ in the 1998 ancestors bar of FIG. 11 Class I recall
  • K982994Skull Base Instatrak SystemVisualization Technology, Inc. · 1998 · 4 generations back · ◆ in the 1998 ancestors bar of FIG. 11 Class I recall
  • K981998Pediatric Instatrak SystemVisualization Technology, Inc. · 1998 · 4 generations back · ◆ in the 1998 ancestors bar of FIG. 11 Class I recall
  • K960330InstatrakVisualization Technology, Inc. · 1996 · 4 generations back · ◆ in the 1996 ancestors bar of FIG. 11 Class I recall

What does this lineage say?

  • The line of descent spans 19 years and passes through 6 companies; a new generation was cleared every 11 months on median.
  • 39 of the 128 ancestors have a recall of any class; 6 have a Class I recall.
  • Of its descendants, K171926 (Guangzhou Sonostar Technologies Co., Ltd., 2017) has gone furthest, with 1 descendant of its own.
  • 4 other devices also cite its predicate K132768.

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. 2014, 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?

The SonoScape S12 system is a general-purpose ultrasonic imaging instrument intended for use by a qualified physician

for evaluation of Fetal, Abdominal, Pediatric, Small Organ (breast, testes, thyroid), Cephalic(neonatal and adult), Trans-rectal, Trans-vaginal, Peripheral Vascular, Musculo-skeletal (Conventional and Superficial), Cardiac (neonatal and adult), OB/Gyn and Urology.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K142474: S12 Digital Color Doppler 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/K142474

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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