510(k) · Cleared
ClearedAdvantage Windows X-Ray/MR Fusion
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Ge Medical Systems, Inc. · LLZ System, Image Processing, Radiological
Cleared on Aug 1, 2002 as substantially equivalent to K983256 (GE Medical Systems, 1998) and 1 other predicate after a 15-day review. Its family tree reaches back 2 generations to 1994. 1 later device descends from it.
- Decided
- Aug 1, 2002
- Review
- 15 days
- Class
- Class II
- Product code
- LLZ
- Recalls
- None
- Predicates
- 2
Its longest line of descent runs back 2 generations to K941223 (1994). 3 ancestors in all. 1 later device descends from it, 1 citing it directly.
- Root · 2 generations backK941223 Advance Analysis SoftwareGeneral Electric Co. · 1994
- 1 generation backK983256 Advantage Windows (AW) FusionGE Medical Systems · 1998
- This deviceK022310 Advantage Windows X-Ray/MR FusionGe Medical Systems, Inc. · 2002
- Descendant · cites it directly · 0 of its ownK093234 Integrated RegistrationGE Medical Systems SCS · 2009
Most influential descendants
Showing 1 of 1 · See all- K093234Integrated RegistrationGE Medical Systems SCS · 2009 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −2 | K941223 | Advance Analysis Software | General Electric Co. | 1994 | — |
| −1 | K983256 | Advantage Windows (AW) Fusion | GE Medical Systems | 1998 | — |
| 0 (this device) | K022310 | Advantage Windows X-Ray/MR Fusion | Ge Medical Systems, Inc. | 2002 | — |
| +1 | K093234 | Integrated Registration | GE Medical Systems SCS | 2009 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2001 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2009 | 1 | 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 LLZ? 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 LLZ device
- #1 K230955 syngo Application Softwarescore 21.5 · 11 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the 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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K983256 | Advantage Windows (AW) FusionSummary page 1…del: Advantage Windows Fusion (CTMR Fusion) Manufacturer: General Electric Medical Systems, Milwaukee, WI 510(k) #: K983256 Model: Advantage Windows Fusion (CTPET Fusion) Manufacturer: General Electric Medical Sy… | 1998 |
| * | K010336 | Advantage Windows CT/Pet Fusion | 2001 |
What descends from it? (1)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K093234 | Integrated Registration | 2009 | 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?
- The line of descent spans 8 years and passes through 3 companies; a new generation was cleared every 4.0 years on median.
- 1 of the 3 ancestors has a recall of any class.
- Of its descendants, K093234 (GE Medical Systems SCS, 2009) has gone furthest, with 0 descendants of its own.
- 5 other devices also cite its predicate K983256.
How does its category compare?
All LLZ devicesLLZ System, Image Processing, Radiological: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · LLZ
58in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · LLZ
173in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · LLZ
11in 2025
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · LLZ
116in 2025
MAUDE reports naming product code LLZ, 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 | 76 | 36 | 20 | 152 |
| 2008 | 94 | 52 | 32 | 154 |
| 2009 | 70 | 62 | 21 | 145 |
| 2010 | 51 | 98 | 17 | 145 |
| 2011 | 106 | 79 | 30 | 454 |
| 2012 | 82 | 87 | 12 | 266 |
| 2013 | 95 | 84 | 64 | 1,130 |
| 2014 | 78 | 89 | 6 | 15,631 |
| 2015 | 64 | 90 | 16 | 211 |
| 2016 | 82 | 90 | 12 | 290 |
| 2017 | 78 | 107 | 5 | 104 |
| 2018 | 104 | 105 | 7 | 72 |
| 2019 | 74 | 107 | 2 | 88 |
| 2020 | 81 | 115 | 6 | 82 |
| 2021 | 83 | 116 | 3 | 70 |
| 2022 | 65 | 137 | 4 | 28 |
| 2023 | 87 | 157 | 8 | 26 |
| 2024 | 62 | 131 | 6 | 42 |
| 2025 | 58 | 173 | 11 | 116 |
| 2026 | 45 | 110 | 14 | — |
What is it indicated for?
Advantage Windows MR Fusion provides an easy means for comparison of three dimensional (3D) images from X-ray angiography (XR: providing anatomical imaging) and Magnetic Resonance (MR: providing anatomical imaging). It allows registration between two volumetric acquisitions, which may come from different acquisition modalities (X-Ray and MR), to help physicians in diagnostic radiology or therapy planning.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K022310 · printed Nov 6, 2026
Cite this page
510(k) Report. “K022310: Advantage Windows X-Ray/MR Fusion.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K022310
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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