510(k) · Cleared
ClearedRT2800(115V)/H4008C and RT2800(220/240V)/H4008CE
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
General Electric Co. · ITX Transducer, Ultrasonic, Diagnostic
Cleared on Feb 10, 1987 after a 140-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 2 of the 673 devices in its family, counting itself, have a Class I recall. 672 later devices descend from it.
- Decided
- Feb 10, 1987
- Review
- 140 days
- Class
- Class II
- Product code
- ITX
- Recalls
- None
- Predicates
- 0
672 later devices descend from it, 2 citing it directly. 2 of the 673 devices in this family, counting this one, have a Class I recall.
- This deviceK863700 RT2800(115V)/H4008C and RT2800(220/240V)/H4008CEGeneral Electric Co. · 1987
- Descendant · cites it directly · 669 of its ownK953752 RT55 Diagnostic Ultrasound SystemGeneral Electric Co. · 1996
- Descendant · 2 generations on · 668 of its ownK012560 GE Logiq A100 MP, Model 2272413General Electric Co. · 2001
- Descendant · 2 generations on · 667 of its ownK014206 LogiqbookGeneral Electric Co. · 2002 · Recalled
- Descendant · 3 generations on · 666 of its ownK032477 GE Logiq BookGeneral Electric Co. · 2003
- Descendant · 3 generations on · 665 of its ownK050126 GE Logiq TwinGeneral Electric Co. · 2005
Showing 5 of 672 descendants. See all descendants
Descendants cleared per year
Class I recalls in this family
Most influential descendants
Showing 5 of 672 · See all- K953752RT55 Diagnostic Ultrasound SystemGeneral Electric Co. · 1996 · cites it directly669descendants
- K012560GE Logiq A100 MP, Model 2272413General Electric Co. · 2001 · 2 generations on668descendants
- K014206LogiqbookGeneral Electric Co. · 2002 · 2 generations on667descendants
- K032477GE Logiq BookGeneral Electric Co. · 2003 · 3 generations on666descendants
- K050126GE Logiq TwinGeneral Electric Co. · 2005 · 3 generations on665descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| 0 (this device) | K863700 | RT2800(115V)/H4008C and RT2800(220/240V)/H4008CE | General Electric Co. | 1987 | — |
| +1 | K953752 | RT55 Diagnostic Ultrasound System | General Electric Co. | 1996 | — |
| +2 | K012560 | GE Logiq A100 MP, Model 2272413 | General Electric Co. | 2001 | — |
| +2 | K014206 | Logiqbook | General Electric Co. | 2002 | 1 |
| +3 | K032477 | GE Logiq Book | General Electric Co. | 2003 | — |
| +3 | K050126 | GE Logiq Twin | General Electric Co. | 2005 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1996 | 2 | 0 |
| 1999 | 1 | 0 |
| 2001 | 1 | 0 |
| 2002 | 1 | 0 |
| 2003 | 1 | 0 |
| 2005 | 1 | 0 |
| 2007 | 1 | 0 |
| 2008 | 4 | 0 |
| 2009 | 5 | 0 |
| 2010 | 9 | 0 |
| 2011 | 13 | 0 |
| 2012 | 16 | 0 |
| 2013 | 20 | 0 |
| 2014 | 29 | 0 |
| 2015 | 39 | 0 |
| 2016 | 42 | 0 |
| 2017 | 64 | 0 |
| 2018 | 49 | 0 |
| 2019 | 37 | 0 |
| 2020 | 57 | 0 |
| 2021 | 45 | 0 |
| 2022 | 46 | 0 |
| 2023 | 38 | 0 |
| 2024 | 50 | 0 |
| 2025 | 58 | 2 |
| 2026 | 43 | 0 |
Sources: FDA 510(k) database (decision fields), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
2 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 ITX device
- #1 K260114 Align® Cover and Pad Guidance Toolscore 13.6 · 6 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against?
FDA has not posted a summary or statement for it, so its predicates are not known.
What descends from it? (672)
See all 6722 later devices cite it directly; ranked here by how many devices descend from each in turn.
Has anything in its family been recalled? (2 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.
What does this lineage say?
- Of its descendants, K953752 (General Electric Co., 1996) has gone furthest, with 669 descendants of its own.
How does its category compare?
All ITX devicesITX Transducer, Ultrasonic, Diagnostic: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · ITX
4in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · ITX
126in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · ITX
2in 2025
Class I (10 since 2007) Class II/III not classified
Adverse event reports per year · ITX
571in 2025
MAUDE reports naming product code ITX, 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 | 10 | 26 | 0 | 16 |
| 2008 | 12 | 73 | 4 | 39 |
| 2009 | 17 | 28 | 4 | 23 |
| 2010 | 10 | 42 | 4 | 30 |
| 2011 | 10 | 16 | 1 | 34 |
| 2012 | 7 | 25 | 1 | 29 |
| 2013 | 3 | 105 | 0 | 38 |
| 2014 | 4 | 41 | 1 | 43 |
| 2015 | 1 | — | 5 | 183 |
| 2016 | 4 | 151 | 0 | 269 |
| 2017 | 6 | 110 | 1 | 412 |
| 2018 | 2 | — | 15 | 130 |
| 2019 | 1 | — | 0 | 119 |
| 2020 | 3 | 120 | 3 | 116 |
| 2021 | 3 | 139 | 10 (10) | 146 |
| 2022 | 2 | — | 6 | 87 |
| 2023 | 6 | 213 | 1 | 138 |
| 2024 | 3 | 81 | 1 | 988 |
| 2025 | 4 | 126 | 2 | 571 |
| 2026 | 6 | 158 | 0 | — |
https://510kreport.com/device/K863700 · printed Nov 5, 2026
Cite this page
510(k) Report. “K863700: RT2800(115V)/H4008C and RT2800(220/240V)/H4008CE.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K863700
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Record history
- FDA decision record loaded May 2, 2026
- Lineage and recalls computed Nov 3, 2026
- Page last updated Nov 3, 2026