510(k) · Cleared
ClearedS6 Diagnostic Ultrasound System
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Sonoscape Company Limited · IYN System, Imaging, Pulsed Doppler, Ultrasonic
Cleared on Nov 7, 2011 after a 61-day review. The summary cites one number, which could not be confirmed as its predicate (see the table below). 36 later devices descend from it.
- Decided
- Nov 7, 2011
- Review
- 61 days
- Class
- Class II
- Product code
- IYN
- Recalls
- None
- Predicates
- 1
36 later devices descend from it, 5 citing it directly.
- This deviceK112602 S6 Diagnostic Ultrasound SystemSonoscape Company Limited · 2011
- Descendant · cites it directly · 32 of its ownK131088 Portable Digital Color Doppler Ultrasound SystemSonoscape Company Limited · 2013
- Descendant · 2 generations on · 30 of its ownK132768 S8 Exp Portable Digital Color Doppler Ultrasound SystemSonoscape Company Limited · 2013
- Descendant · 2 generations on · 19 of its ownK142710 S9 Portable Digital Color Doppler Ultrasound SystemSonoscape Company Limited · 2015
- Descendant · cites it directly · 18 of its ownK131213 Digital Color Doppler Ultrasound SystemSonoscape Company Limited · 2013
- Descendant · 2 generations on · 17 of its ownK150045 S30/S40 Digital Color Doppler Ultraound SystemSonoscape Company Limited · 2015
Showing 5 of 36 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 36 · See all- K131088Portable Digital Color Doppler Ultrasound SystemSonoscape Company Limited · 2013 · cites it directly32descendants
- K132768S8 Exp Portable Digital Color Doppler Ultrasound SystemSonoscape Company Limited · 2013 · 2 generations on30descendants
- K142710S9 Portable Digital Color Doppler Ultrasound SystemSonoscape Company Limited · 2015 · 2 generations on19descendants
- K131213Digital Color Doppler Ultrasound SystemSonoscape Company Limited · 2013 · cites it directly18descendants
- K150045S30/S40 Digital Color Doppler Ultraound SystemSonoscape Company Limited · 2015 · 2 generations on17descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| 0 (this device) | K112602 | S6 Diagnostic Ultrasound System | Sonoscape Company Limited | 2011 | — |
| +1 | K131088 | Portable Digital Color Doppler Ultrasound System | Sonoscape Company Limited | 2013 | — |
| +2 | K132768 | S8 Exp Portable Digital Color Doppler Ultrasound System | Sonoscape Company Limited | 2013 | — |
| +2 | K142710 | S9 Portable Digital Color Doppler Ultrasound System | Sonoscape Company Limited | 2015 | — |
| +1 | K131213 | Digital Color Doppler Ultrasound System | Sonoscape Company Limited | 2013 | — |
| +2 | K150045 | S30/S40 Digital Color Doppler Ultraound System | Sonoscape Company Limited | 2015 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2013 | 5 | 0 |
| 2014 | 1 | 0 |
| 2015 | 7 | 0 |
| 2016 | 3 | 0 |
| 2017 | 9 | 0 |
| 2019 | 1 | 0 |
| 2020 | 1 | 0 |
| 2022 | 3 | 0 |
| 2023 | 1 | 0 |
| 2024 | 1 | 0 |
| 2025 | 2 | 0 |
| 2026 | 2 | 0 |
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 K240850 EPIQ Series Diagnostic Ultrasound Systems…score 32.1 · 24 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the 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; numbers the summary cites that cannot be its predicate are marked – and kept off the family tree.
| Type | Number | Device | Decided |
|---|---|---|---|
| Kept off the family tree | K1110510 | S20 Digital Doppler Ultrasound System and Transducers Number could not be read |
What descends from it? (36)
See all 365 later devices cite it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K131088 | Portable Digital Color Doppler Ultrasound System | 2013 | 32 |
| K131213 | Digital Color Doppler Ultrasound System | 2013 | 18 |
| K130801 | Digital Color Doppler Ultrasound System | 2013 | 1 |
| K170078 | Medisono Color Doppler Ultrasound System, models P11 Portable, P11 EXPERT Portable, P12… | 2017 | 0 |
| K130119 | Portable Digital Color Doppler Ultrasound System | 2013 | 0 |
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?
- Of its descendants, K131088 (Sonoscape Company Limited, 2013) has gone furthest, with 32 descendants of its own.
How does its category compare?
All IYN devicesIYN 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
2026 to Oct 25, outlined.
Median 510(k) review, days · IYN
124in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · IYN
10in 2025
Class I (1 since 2007) Class II/III not classified
Adverse event reports per year · IYN
610in 2025
MAUDE reports naming product code IYN, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 13 | 26 | 16 | 3 |
| 2008 | 25 | 18 | 12 | 2 |
| 2009 | 18 | 29 | 8 | 9 |
| 2010 | 29 | 67 | 10 | 17 |
| 2011 | 39 | 46 | 8 | 18 |
| 2012 | 43 | 37 | 3 | 20 |
| 2013 | 51 | 60 | 8 | 18 |
| 2014 | 56 | 39 | 2 | 48 |
| 2015 | 54 | 55 | 3 | 116 |
| 2016 | 60 | 56 | 2 | 145 |
| 2017 | 64 | 83 | 0 | 146 |
| 2018 | 59 | 85 | 7 | 85 |
| 2019 | 47 | 79 | 0 | 59 |
| 2020 | 57 | 72 | 4 | 67 |
| 2021 | 46 | 105 | 8 | 213 |
| 2022 | 53 | 105 | 10 | 186 |
| 2023 | 44 | 115 | 4 | 229 |
| 2024 | 50 | 119 | 1 | 266 |
| 2025 | 57 | 124 | 10 | 610 |
| 2026 | 44 | 107 | 2 (1) | — |
What is it indicated for?
The SonoScape S6 device 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.
https://510kreport.com/device/K112602 · printed Nov 6, 2026
Cite this page
510(k) Report. “K112602: S6 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/K112602
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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