510(k) Report

510(k) · Cleared

Cleared

Accuvix XG Diagnostic Ultrasound System

K103397510(k) TraditionalCleared Feb 25, 201198-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

Medison Co., Ltd. · IYN System, Imaging, Pulsed Doppler, Ultrasonic

Cleared on Feb 25, 2011 as substantially equivalent to K101455 (Medison Co., Ltd., 2010) and 1 other predicate after a 98-day review. Its family tree reaches back 13 generations to 1993. 110 later devices descend from it.

Decided
Feb 25, 2011
Review
98 days
Class
Class II
Product code
IYN
Recalls
None
Predicates
2

Its longest line of descent runs back 13 generations to K924432 (1993). 23 ancestors in all. 110 later devices descend from it, 6 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2002: 1 other ancestor2001: 1 other ancestor2000: 1 other ancestor1999: 2 other ancestors1998: 2 other ancestors1997: 2 other ancestors1994: 1 other ancestor2013: 5 descendants cleared2015: 5 descendants cleared2014: 4 descendants cleared2011: 1 descendant cleared2012: 1 descendant cleared2017: 10 descendants cleared2019: 11 descendants cleared2016: 6 descendants cleared2018: 11 descendants cleared2023: 8 descendants cleared2020: 7 descendants cleared2021: 11 descendants cleared2022: 11 descendants cleared2025: 8 descendants cleared2024: 6 descendants cleared2026: 5 descendants clearedK924432 · Medison 1500 · Medison Co., Ltd. · 1993K981510 · Sonoace 6000/ Ultramark 400 · Medison America, Inc. · 1998K990970 · Sonoace 6000C Diagnostic Ultrasound System and Transducers, Also Called Ultrasound System and Transducers · Medison America, Inc. · 1999K002185 · Sonoace SA 9900 Diagnostic Ultrasound System · Medison America, Inc. · 2000 · recalledK013627 · Sonoace SA-8000 Diagnostic Ultrasound System · Medison America, Inc. · 2001K032329 · SA 9900 Plus Diagnostic Ultrasound System · Medison America, Inc. · 2003K052911 · Accuvix XQ Diagnostic Ultrasound System · Medison Co., Ltd. · 2005×2: 2 generations cleared close together, K063580 (2006), K070813 (2007) K080800 · Accuvix V20 Diagnostic Ultrasound System · Medison Co., Ltd. · 2008K092159 · Accuvix V20 Diagnostic Ultrasound System · Medison Co., Ltd. · 2009K093849 · Accuvix V10 Diagnostic Ultrasound System · Medison Co., Ltd. · 2010K101455 · Eko 7 Diagnostic Ultrasound System · Medison Co., Ltd. · 20101990200020102020
Other ancestors, by generationDescendants, by generation 2 generations back: 1 other ancestor3 generations back: 2 other ancestors4 generations back: 4 other ancestors5 generations back: 2 other ancestors6 generations back: 1 other ancestor 1 generation forward: 6 descendants2 generations forward: 12 descendants3 generations forward: 16 descendants4 generations forward: 18 descendants5 generations forward: 19 descendants6 generations forward: 12 descendants7 generations forward: 11 descendants8 generations forward: 7 descendants9 generations forward: 3 descendants10 generations forward: 3 descendants11 generations forward: 2 descendants12 generations forward: 1 descendant K101455 · Eko 7 Diagnostic Ultrasound System · Medison Co., Ltd. · 2010K093849 · Accuvix V10 Diagnostic Ultrasound System · Medison Co., Ltd. · 2010K092159 · Accuvix V20 Diagnostic Ultrasound System · Medison Co., Ltd. · 2009K080800 · Accuvix V20 Diagnostic Ultrasound System · Medison Co., Ltd. · 2008K070813 · Accuvix V10 Diagnostic Ultrasound System · Medison Co., Ltd. · 2007K063580 · Sonoace X8 Diagnostic Ultrasound System · Medison Co., Ltd. · 2006K052911 · Accuvix XQ Diagnostic Ultrasound System · Medison Co., Ltd. · 2005K032329 · SA 9900 Plus Diagnostic Ultrasound System · Medison America, Inc. · 2003K013627 · Sonoace SA-8000 Diagnostic Ultrasound System · Medison America, Inc. · 2001K002185 · Sonoace SA 9900 Diagnostic Ultrasound System · Medison America, Inc. · 2000 · recalledK990970 · Sonoace 6000C Diagnostic Ultrasound System and Transducers, Also Called Ultrasound System and Transducers · Medison America, Inc. · 1999K981510 · Sonoace 6000/ Ultramark 400 · Medison America, Inc. · 1998K924432 · Medison 1500 · Medison Co., Ltd. · 1993−10−50+5+10
  1. Root · 13 generations backK924432 Medison 1500Medison Co., Ltd. · 1993
  2. 9 generations between
  3. 3 generations backK092159 Accuvix V20 Diagnostic Ultrasound SystemMedison Co., Ltd. · 2009
  4. 2 generations backK093849 Accuvix V10 Diagnostic Ultrasound SystemMedison Co., Ltd. · 2010
  5. 1 generation backK101455 Eko 7 Diagnostic Ultrasound SystemMedison Co., Ltd. · 2010
  6. This deviceK103397 Accuvix XG Diagnostic Ultrasound SystemMedison Co., Ltd. · 2011
  7. Descendant · cites it directly · 109 of its ownK112339 Accuvix A30 Diagnostic Ultrasound SystemSamsung Medison Co., Ltd. · 2011
  8. Descendant · 2 generations on · 108 of its ownK122583 Ugeo G60 Diagnostic Ultrasound SystemSamsung Medison Co., Ltd. · 2012
  9. Descendant · 2 generations on · 106 of its ownK130803 Ugeo H70C Diagnostic Ultrasound SystemSamsung Medison Co., Ltd. · 2013
  10. Descendant · cites it directly · 102 of its ownK133329 Ugeo WS80A Diagnostic Ultrasound SystemSamsung Medison Co., Ltd. · 2013
  11. Descendant · 3 generations on · 102 of its ownK132861 Ugeo H60 Diagnostic Ultrasound SystemSamsung Medison Co., Ltd. · 2013
Show all 13 generations
  1. Root · 13 generations backK924432 Medison 1500Medison Co., Ltd. · 1993
  2. 12 generations backK981510 Sonoace 6000/ Ultramark 400Medison America, Inc. · 1998
  3. 11 generations backK990970 Sonoace 6000C Diagnostic Ultrasound System and Transducers, Also…Medison America, Inc. · 1999
  4. 10 generations backK002185 Sonoace SA 9900 Diagnostic Ultrasound SystemMedison America, Inc. · 2000 · Recalled
  5. 9 generations backK013627 Sonoace SA-8000 Diagnostic Ultrasound SystemMedison America, Inc. · 2001
  6. 8 generations backK032329 SA 9900 Plus Diagnostic Ultrasound SystemMedison America, Inc. · 2003
  7. 7 generations backK052911 Accuvix XQ Diagnostic Ultrasound SystemMedison Co., Ltd. · 2005
  8. 6 generations backK063580 Sonoace X8 Diagnostic Ultrasound SystemMedison Co., Ltd. · 2006
  9. 5 generations backK070813 Accuvix V10 Diagnostic Ultrasound SystemMedison Co., Ltd. · 2007
  10. 4 generations backK080800 Accuvix V20 Diagnostic Ultrasound SystemMedison Co., Ltd. · 2008
  11. 3 generations backK092159 Accuvix V20 Diagnostic Ultrasound SystemMedison Co., Ltd. · 2009
  12. 2 generations backK093849 Accuvix V10 Diagnostic Ultrasound SystemMedison Co., Ltd. · 2010
  13. 1 generation backK101455 Eko 7 Diagnostic Ultrasound SystemMedison Co., Ltd. · 2010
  14. This deviceK103397 Accuvix XG Diagnostic Ultrasound SystemMedison Co., Ltd. · 2011

Showing 5 of 110 descendants. See all descendants

Descendants cleared per year

2011: 12012: 12013: 52014: 42015: 52016: 62017: 102018: 112019: 112020: 72021: 112022: 112023: 82024: 62025: 82026: 5
2011high 11 (2018) · low 1 (2011)2026

Most influential descendants

Showing 5 of 110 · See all
  • K112339Accuvix A30 Diagnostic Ultrasound SystemSamsung Medison Co., Ltd. · 2011 · cites it directly109descendants
  • K122583Ugeo G60 Diagnostic Ultrasound SystemSamsung Medison Co., Ltd. · 2012 · 2 generations on108descendants
  • K130803Ugeo H70C Diagnostic Ultrasound SystemSamsung Medison Co., Ltd. · 2013 · 2 generations on106descendants
  • K133329Ugeo WS80A Diagnostic Ultrasound SystemSamsung Medison Co., Ltd. · 2013 · cites it directly102descendants
  • K132861Ugeo H60 Diagnostic Ultrasound SystemSamsung Medison Co., Ltd. · 2013 · 3 generations on102descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−13K924432Medison 1500Medison Co., Ltd.1993—
−12K981510Sonoace 6000/ Ultramark 400Medison America, Inc.1998—
−11K990970Sonoace 6000C Diagnostic Ultrasound System and Transducers, Also Called…Medison America, Inc.1999—
−10K002185Sonoace SA 9900 Diagnostic Ultrasound SystemMedison America, Inc.20001
−9K013627Sonoace SA-8000 Diagnostic Ultrasound SystemMedison America, Inc.2001—
−8K032329SA 9900 Plus Diagnostic Ultrasound SystemMedison America, Inc.2003—
−7K052911Accuvix XQ Diagnostic Ultrasound SystemMedison Co., Ltd.2005—
−6K063580Sonoace X8 Diagnostic Ultrasound SystemMedison Co., Ltd.2006—
−5K070813Accuvix V10 Diagnostic Ultrasound SystemMedison Co., Ltd.2007—
−4K080800Accuvix V20 Diagnostic Ultrasound SystemMedison Co., Ltd.2008—
−3K092159Accuvix V20 Diagnostic Ultrasound SystemMedison Co., Ltd.2009—
−2K093849Accuvix V10 Diagnostic Ultrasound SystemMedison Co., Ltd.2010—
−1K101455Eko 7 Diagnostic Ultrasound SystemMedison Co., Ltd.2010—
0 (this device)K103397Accuvix XG Diagnostic Ultrasound SystemMedison Co., Ltd.2011—
+1K112339Accuvix A30 Diagnostic Ultrasound SystemSamsung Medison Co., Ltd.2011—
+2K122583Ugeo G60 Diagnostic Ultrasound SystemSamsung Medison Co., Ltd.2012—
+2K130803Ugeo H70C Diagnostic Ultrasound SystemSamsung Medison Co., Ltd.2013—
+1K133329Ugeo WS80A Diagnostic Ultrasound SystemSamsung Medison Co., Ltd.2013—
+3K132861Ugeo H60 Diagnostic Ultrasound SystemSamsung Medison Co., Ltd.2013—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199410
199720
199820
199920
200010
200110
200210

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201110
201210
201350
201440
201550
201660
2017100
2018110
2019110
202070
2021110
2022110
202380
202460
202580
202650
FIG. 1 — Lineage of K103397, 1993–2026Source: 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? (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
*K101455Eko 7 Diagnostic Ultrasound System
Summary page 2
…cleared via K092159, and the EKO 7 Diagnostic Ultrasound System, cleared via K 101455. All systems transmit ultrasonic energy into patients, then perform post processing of received…
Medison Co., Ltd.2010—
*K092159Accuvix V20 Diagnostic Ultrasound System
Summary page 1
…cer 892.1570 ITX 3. Identification of the predicate or legally marketed device: KID0 1455, EKO 7 Diagnostic Ultrasound System K092 159, ACCUVIX V20 Diagnostic Ultrasound System 510(k) Summary /Statement Certification…
Medison Co., Ltd.2009—

Also cleared against K101455: 2 other devices →

What descends from it? (110)

See all 110

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

NumberDeviceApplicantDecidedDescendants
K112339Accuvix A30 Diagnostic Ultrasound SystemSamsung Medison Co., Ltd.2011109
K133329Ugeo WS80A Diagnostic Ultrasound SystemSamsung Medison Co., Ltd.2013102
K141620RS80A Diagnostic Ultrasound SystemSamsung Medison Co., Ltd.2014101
K142466UGEO PT60A Diagnostic Ultrasound SystemSamsung Medison Co., Ltd.201499
K152962HS70A Diagnostic Ultrasound SystemSamsung Medison Co., Ltd.201590
K153408HM70A Diagnostic Ultrasound SystemSamsung Medison Co., Ltd.201565

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 18 years and passes through 2 companies; a new generation was cleared every 1.1 years on median.
  • 1 of the 23 ancestors has a recall of any class.
  • Of its descendants, K112339 (Samsung Medison Co., Ltd., 2011) has gone furthest, with 109 descendants of its own.
  • 2 other devices also cite its predicate K101455.

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. 2011, 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 ACCUVIX XG Diagnostic Ultrasound System and transducers are intended for diagnostic ultrasound imaging and fluid analysis of the human body.

The clinical applications include: Fetal, Abdominal, Intra-operative, Pediatric, Small Organ, Neonatal Cephalic, Adult Cephalic, Trans-rectal, Trans-vaginal, Muscular-Skeletal (Conventional, Superficial), Cardiac Adult, Cardiac Pediatric, Peripheral vessel

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. “K103397: Accuvix XG Diagnostic Ultrasound System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K103397

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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