510(k) · Cleared
ClearedAdvantage V.S. CT/MR Rad Diagnostic Workstation
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
General Electric Co. · LNH System, Nuclear Magnetic Resonance Imaging
Cleared on Dec 27, 1991 after a 127-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 3 of the 1,149 devices in its family, counting itself, have a Class I recall. 1,148 later devices descend from it.
- Decided
- Dec 27, 1991
- Review
- 127 days
- Class
- Class II
- Product code
- LNH
- Recalls
- None
- Predicates
- 0
1,148 later devices descend from it, 4 citing it directly. 3 of the 1,149 devices in this family, counting this one, have a Class I recall.
- This deviceK913770 Advantage V.S. CT/MR Rad Diagnostic WorkstationGeneral Electric Co. · 1991
- Descendant · cites it directly · 914 of its ownK960613 GE Advantage Windows Review WorkstationGE Medical Systems · 1996
- Descendant · 2 generations on · 872 of its ownK020483 Advantage Workstation 4.1GE Medical Systems · 2002 · Recalled
- Descendant · 3 generations on · 637 of its ownK033400 Seno AdvantageGe Medical Systems W-400 · 2003 · Recalled
- Descendant · cites it directly · 472 of its ownK963345 Advantage Windows Tissue Volume OptionGE Medical Systems · 1996
- Descendant · 2 generations on · 470 of its ownK013381 Advanced Lung Analysis-1General Electric Co. · 2001
Showing 5 of 1,148 descendants. See all descendants
Descendants cleared per year
Class I recalls in this family
Most influential descendants
Showing 5 of 1,148 · See all- K960613GE Advantage Windows Review WorkstationGE Medical Systems · 1996 · cites it directly914descendants
- K020483Advantage Workstation 4.1GE Medical Systems · 2002 · 2 generations on872descendants
- K033400Seno AdvantageGe Medical Systems W-400 · 2003 · 3 generations on637descendants
- K963345Advantage Windows Tissue Volume OptionGE Medical Systems · 1996 · cites it directly472descendants
- K013381Advanced Lung Analysis-1General Electric Co. · 2001 · 2 generations on470descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| 0 (this device) | K913770 | Advantage V.S. CT/MR Rad Diagnostic Workstation | General Electric Co. | 1991 | — |
| +1 | K960613 | GE Advantage Windows Review Workstation | GE Medical Systems | 1996 | — |
| +2 | K020483 | Advantage Workstation 4.1 | GE Medical Systems | 2002 | 2 |
| +3 | K033400 | Seno Advantage | Ge Medical Systems W-400 | 2003 | 6 |
| +1 | K963345 | Advantage Windows Tissue Volume Option | GE Medical Systems | 1996 | — |
| +2 | K013381 | Advanced Lung Analysis-1 | General Electric Co. | 2001 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1996 | 3 | 0 |
| 1997 | 1 | 0 |
| 1998 | 7 | 0 |
| 1999 | 2 | 0 |
| 2001 | 2 | 0 |
| 2002 | 6 | 0 |
| 2003 | 10 | 0 |
| 2004 | 19 | 0 |
| 2005 | 18 | 0 |
| 2006 | 21 | 0 |
| 2007 | 23 | 0 |
| 2008 | 24 | 0 |
| 2009 | 25 | 0 |
| 2010 | 16 | 0 |
| 2011 | 34 | 0 |
| 2012 | 44 | 0 |
| 2013 | 37 | 0 |
| 2014 | 44 | 0 |
| 2015 | 50 | 1 |
| 2016 | 46 | 0 |
| 2017 | 56 | 1 |
| 2018 | 71 | 0 |
| 2019 | 54 | 0 |
| 2020 | 66 | 0 |
| 2021 | 73 | 0 |
| 2022 | 71 | 0 |
| 2023 | 68 | 0 |
| 2024 | 83 | 0 |
| 2025 | 93 | 1 |
| 2026 | 81 | 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.
3 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 LNH device
- #1 K213693 MAGNETOM Vida with syngo MR XA50Ascore 23.0 · 18 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? (1,148)
See all 1,1484 later devices cite it directly; ranked here by how many devices descend from each in turn.
Has anything in its family been recalled? (3 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.
- K143457NeuroBlate SystemMonteris Medical, Inc. · 2015 · 7 generations on · ◆ in the 2015 descendants bar of FIG. 11 Class I recall
- K171255Monteris Medical NeuroBlate SystemMonteris Medical, Inc. · 2017 · 7 generations on · ◆ in the 2017 descendants bar of FIG. 11 Class I recall
- K250443MAGNETOM Avanto Fit; MAGNETOM Skyra Fit; MAGNETOM Sola Fit; MAGNETOM Viato.MobileSiemens Healthcare GmbH · 2025 · 8 generations on · ◆ in the 2025 descendants bar of FIG. 12 Class I recalls
What does this lineage say?
- Of its descendants, K960613 (GE Medical Systems, 1996) has gone furthest, with 914 descendants of its own.
How does its category compare?
All LNH devicesLNH System, Nuclear Magnetic Resonance Imaging: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · LNH
26in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · LNH
122in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · LNH
8in 2025
Class I (8 since 2007) Class II/III not classified
Adverse event reports per year · LNH
1,263in 2025
MAUDE reports naming product code LNH, 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 | 12 | 35 | 25 | 114 |
| 2008 | 19 | 53 | 12 | 167 |
| 2009 | 17 | 70 | 7 | 194 |
| 2010 | 12 | 94 | 17 | 165 |
| 2011 | 16 | 81 | 11 | 182 |
| 2012 | 22 | 89 | 5 | 170 |
| 2013 | 19 | 108 | 2 | 107 |
| 2014 | 17 | 108 | 13 | 119 |
| 2015 | 19 | 140 | 12 (2) | 113 |
| 2016 | 20 | 108 | 1 | 135 |
| 2017 | 18 | 98 | 0 | 121 |
| 2018 | 29 | 128 | 71 | 158 |
| 2019 | 26 | 62 | 5 | 158 |
| 2020 | 32 | 121 | 4 | 98 |
| 2021 | 27 | 87 | 41 | 84 |
| 2022 | 30 | 74 | 13 | 138 |
| 2023 | 30 | 124 | 10 (1) | 159 |
| 2024 | 26 | 104 | 4 | 281 |
| 2025 | 26 | 122 | 8 (5) | 1,263 |
| 2026 | 24 | 126 | 43 | — |
https://510kreport.com/device/K913770 · printed Nov 6, 2026
Cite this page
510(k) Report. “K913770: Advantage V.S. CT/MR Rad Diagnostic Workstation.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K913770
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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