510(k) Report

510(k) · Cleared

Cleared

Aplio XG Diagnostic Ultrasound System, Model Ssa-790A Version 2.0

K072000510(k) TraditionalCleared Jul 30, 20077-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

Toshiba America Medical Systems, In.C · IYN System, Imaging, Pulsed Doppler, Ultrasonic

Cleared on Jul 30, 2007 as substantially equivalent to K063130 (Toshibamedical Systems Corporation, 2006) and 1 other predicate after a 7-day review. Its family tree reaches back 8 generations to 1989. 203 later devices descend from it.

Decided
Jul 30, 2007
Review
7 days
Class
Class II
Product code
IYN
Recalls
None
Predicates
2

Its longest line of descent runs back 8 generations to K894632 (1989). 49 ancestors in all. 203 later devices descend from it, 4 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2005: 2 other ancestors2004: 2 other ancestors2002: 2 other ancestors1999: 6 other ancestors2003: 3 other ancestors2001: 1 other ancestor2000: 3 other ancestors1997: 6 other ancestors1995: 5 other ancestors1998: 2 other ancestors1996: 2 other ancestors1994: 5 other ancestors1992: 1 other ancestor1993: 1 other ancestor2007: 1 descendant cleared2008: 5 descendants cleared2015: 5 descendants cleared2009: 5 descendants cleared2017: 12 descendants cleared2016: 7 descendants cleared2013: 4 descendants cleared2011: 4 descendants cleared2012: 8 descendants cleared2018: 18 descendants cleared2010: 1 descendant cleared2014: 10 descendants cleared2019: 8 descendants cleared2023: 18 descendants cleared2025: 26 descendants cleared2020: 20 descendants cleared2021: 9 descendants cleared2026: 13 descendants cleared2022: 16 descendants cleared2024: 13 descendants clearedK894632 · Model SSH-140A Ultrasound Imaging System · Toshiba America Medical Systems, In.C · 1989K941593 · Diagnostic Ultrasonic Transducer · Toshiba America Medical Systems, In.C · 1996K970047 · Phased Array Transducer - - PSK-20CT · Toshiba America Medical Systems, In.C · 1997K991858 · Ssa-390A/Power Vision 8000 · Toshiba America Medical Systems, In.C · 1999K013633 · Ssa-770A, Aplio Ultrasound System · Toshiba America Medical Systems, In.C · 2001K022400 · Ssa-700A, Aplio Diagnostic Ultrasound System · Toshiba America Medical Systems, In.C · 2002 · recalledK032281 · Ssa-770A - Version 4, Aplio Diagnostic Ultrasound System · Toshiba America Medical Systems, In.C · 2003K063130 · Aplio XG Diagnostic Ultrasound System, Model Ssa-790A, Version 1.0 · Toshibamedical Systems Corporation · 2006 · recalled1990200020102020
Other ancestors, by generationDescendants, by generation 1 generation back: 1 other ancestor2 generations back: 1 other ancestor3 generations back: 5 other ancestors4 generations back: 14 other ancestors5 generations back: 11 other ancestors6 generations back: 6 other ancestors7 generations back: 3 other ancestors 1 generation forward: 4 descendants2 generations forward: 7 descendants3 generations forward: 7 descendants4 generations forward: 15 descendants5 generations forward: 23 descendants6 generations forward: 21 descendants7 generations forward: 31 descendants8 generations forward: 25 descendants9 generations forward: 21 descendants10 generations forward: 19 descendants11 generations forward: 9 descendants12 generations forward: 7 descendants13 generations forward: 7 descendants14 generations forward: 4 descendants15 generations forward: 3 descendants K063130 · Aplio XG Diagnostic Ultrasound System, Model Ssa-790A, Version 1.0 · Toshibamedical Systems Corporation · 2006 · recalledK032281 · Ssa-770A - Version 4, Aplio Diagnostic Ultrasound System · Toshiba America Medical Systems, In.C · 2003K022400 · Ssa-700A, Aplio Diagnostic Ultrasound System · Toshiba America Medical Systems, In.C · 2002 · recalledK013633 · Ssa-770A, Aplio Ultrasound System · Toshiba America Medical Systems, In.C · 2001K991858 · Ssa-390A/Power Vision 8000 · Toshiba America Medical Systems, In.C · 1999K970047 · Phased Array Transducer - - PSK-20CT · Toshiba America Medical Systems, In.C · 1997K941593 · Diagnostic Ultrasonic Transducer · Toshiba America Medical Systems, In.C · 1996K894632 · Model SSH-140A Ultrasound Imaging System · Toshiba America Medical Systems, In.C · 1989−50+5+10+15
  1. Root · 8 generations backK894632 Model SSH-140A Ultrasound Imaging SystemToshiba America Medical Systems, In.C · 1989
  2. 7 generations backK941593 Diagnostic Ultrasonic TransducerToshiba America Medical Systems, In.C · 1996
  3. 6 generations backK970047 Phased Array Transducer - - PSK-20CTToshiba America Medical Systems, In.C · 1997
  4. 5 generations backK991858 Ssa-390A/Power Vision 8000Toshiba America Medical Systems, In.C · 1999
  5. 4 generations backK013633 Ssa-770A, Aplio Ultrasound SystemToshiba America Medical Systems, In.C · 2001
  6. 3 generations backK022400 Ssa-700A, Aplio Diagnostic Ultrasound SystemToshiba America Medical Systems, In.C · 2002 · Recalled
  7. 2 generations backK032281 Ssa-770A - Version 4, Aplio Diagnostic Ultrasound SystemToshiba America Medical Systems, In.C · 2003
  8. 1 generation backK063130 Aplio XG Diagnostic Ultrasound System, Model Ssa-790A, Version 1.0Toshibamedical Systems Corporation · 2006 · Recalled
  9. This deviceK072000 Aplio XG Diagnostic Ultrasound System, Model Ssa-790A Version 2.0Toshiba America Medical Systems, In.C · 2007
  10. Descendant · cites it directly · 181 of its ownK080160 Aplio Artida, Model SSH-880CV Diagnostic Ultrasound SystemToshiba America Medical Systems, In.C · 2008
  11. Descendant · cites it directly · 118 of its ownK081065 Aplio XG Diagnostic Ultrasound System, Model Ssa - 790A, Version 2.2Toshiba America Medical Systems, In.C · 2008
  12. Descendant · 2 generations on · 116 of its ownK082119 Aplio XG Diagnostic Ultrasound System, Model Ssa - 790A Version 3.0Toshiba America Medical Systems, In.C · 2008
  13. Descendant · 2 generations on · 98 of its ownK090158 Aplio Artida V2.0 SSH-880CVToshiba America Medical Systems, In.C · 2009 · Recalled
  14. Descendant · 3 generations on · 89 of its ownK110870 Aplio Diagnostic Ultrasound System; Aplio Diagnostic Ultrasound…Toshiba America Medical Systems, In.C · 2011

Showing 5 of 203 descendants. See all descendants

Descendants cleared per year

2007: 12008: 52009: 52010: 12011: 42012: 82013: 42014: 102015: 52016: 72017: 122018: 182019: 82020: 202021: 92022: 162023: 182024: 132025: 262026: 13
2007high 26 (2025) · low 1 (2007)2026

Most influential descendants

Showing 5 of 203 · See all
  • K080160Aplio Artida, Model SSH-880CV Diagnostic Ultrasound SystemToshiba America Medical Systems, In.C · 2008 · cites it directly181descendants
  • K081065Aplio XG Diagnostic Ultrasound System, Model Ssa - 790A, Version 2.2Toshiba America Medical Systems, In.C · 2008 · cites it directly118descendants
  • K082119Aplio XG Diagnostic Ultrasound System, Model Ssa - 790A Version 3.0Toshiba America Medical Systems, In.C · 2008 · 2 generations on116descendants
  • K090158Aplio Artida V2.0 SSH-880CVToshiba America Medical Systems, In.C · 2009 · 2 generations on98descendants
  • K110870Aplio Diagnostic Ultrasound System; Aplio Diagnostic Ultrasound System; Aplio Diagnostic…Toshiba America Medical Systems, In.C · 2011 · 3 generations on89descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−8K894632Model SSH-140A Ultrasound Imaging SystemToshiba America Medical Systems, In.C1989—
−7K941593Diagnostic Ultrasonic TransducerToshiba America Medical Systems, In.C1996—
−6K970047Phased Array Transducer - - PSK-20CTToshiba America Medical Systems, In.C1997—
−5K991858Ssa-390A/Power Vision 8000Toshiba America Medical Systems, In.C1999—
−4K013633Ssa-770A, Aplio Ultrasound SystemToshiba America Medical Systems, In.C2001—
−3K022400Ssa-700A, Aplio Diagnostic Ultrasound SystemToshiba America Medical Systems, In.C20021
−2K032281Ssa-770A - Version 4, Aplio Diagnostic Ultrasound SystemToshiba America Medical Systems, In.C2003—
−1K063130Aplio XG Diagnostic Ultrasound System, Model Ssa-790A, Version 1.0Toshibamedical Systems Corporation20061
0 (this device)K072000Aplio XG Diagnostic Ultrasound System, Model Ssa-790A Version 2.0Toshiba America Medical Systems, In.C2007—
+1K080160Aplio Artida, Model SSH-880CV Diagnostic Ultrasound SystemToshiba America Medical Systems, In.C2008—
+1K081065Aplio XG Diagnostic Ultrasound System, Model Ssa - 790A, Version 2.2Toshiba America Medical Systems, In.C2008—
+2K082119Aplio XG Diagnostic Ultrasound System, Model Ssa - 790A Version 3.0Toshiba America Medical Systems, In.C2008—
+2K090158Aplio Artida V2.0 SSH-880CVToshiba America Medical Systems, In.C20095
+3K110870Aplio Diagnostic Ultrasound System; Aplio Diagnostic Ultrasound System; Aplio…Toshiba America Medical Systems, In.C2011—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199210
199310
199450
199550
199620
199760
199820
199960
200030
200110
200220
200330
200420
200520

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200710
200850
200950
201010
201140
201280
201340
2014100
201550
201670
2017120
2018180
201980
2020200
202190
2022160
2023180
2024130
2025260
2026130
FIG. 1 — Lineage of K072000, 1989–2026Source: 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
*K063130Aplio XG Diagnostic Ultrasound System, Model Ssa-790A, Version 1.0
Summary page 1
…al Systems believes that this device is substantially equivalent to: 1I) Toshiba SSA-790A, Aplio XG Version 1.00 Diagnostic Ultrasound; 510(k) control number k063130 2) Siemens Medical Solutions U.S.A. Acuson Sequoia Ultrasound System;510(k) control number k052410 Device Description…
Toshibamedical Systems Corporation20061
*K052410Acuson Sequoia Ultrasound System
Summary page 1
…n 1.00 Diagnostic Ultrasound; 510(k) control number k063130 2) Siemens Medical Solutions U.S.A. Acuson Sequoia Ultrasound System;510(k) control number k052410 Device Description: The Aplio XG Ultrasound System is a mobile system. This system is a Track 3 device that employs a wide array…
Siemens Medical Solutions USA, Inc.2005—

Also cleared against K063130: 1 other device →

What descends from it? (203)

See all 203

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

NumberDeviceApplicantDecidedDescendants
K080160Aplio Artida, Model SSH-880CV Diagnostic Ultrasound SystemToshiba America Medical Systems, In.C2008181
K081065Aplio XG Diagnostic Ultrasound System, Model Ssa - 790A, Version 2.2Toshiba America Medical Systems, In.C2008118
K151451Aplio 500/400/300 Diagnostic Ultrasound System V6.0Toshibamedical Systems Corporation201534
K072918Model Ssa-680A Xario XG Diagnostic Ultrasound System, Version 1.00Toshibamedical Systems Corporation20070

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 2.3 years on median.
  • 5 of the 49 ancestors have a recall of any class.
  • Of its descendants, K080160 (Toshiba America Medical Systems, In.C, 2008) has gone furthest, with 181 descendants of its own.
  • 1 other device also cites its predicate K063130.

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. 2007, 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 Aplio XG is intended to be used for the following type of studies; fetal, abdominal, intraoperative, pediatric, small organs, neonatal cephalic, adult cephalic, cardiac, transrectal, transvaginal, transesophageal, peripheral vascular and musculo-skeletal (both conventional and superficial).

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K072000: Aplio XG Diagnostic Ultrasound System, Model Ssa-790A Version 2.0.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K072000

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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