510(k) · Cleared
ClearedClearmri Helios-RG8 Coil Accessory Kit
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Clearmri Solutions, Inc. · LNH System, Nuclear Magnetic Resonance Imaging
Cleared on Apr 4, 2014 as substantially equivalent to K962061 (GE Medical Systems, 1996) after a 247-day review. Its family tree reaches back 1 generation to 1996.
- Decided
- Apr 4, 2014
- Review
- 247 days
- Class
- Class II
- Product code
- LNH
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 1 generation to K962061 (1996). No later device cites it as a predicate yet.
- Root · 1 generation backK962061 Magnetic Resonance Diagnostic SystemGE Medical Systems · 1996 · Recalled
- This deviceK132381 Clearmri Helios-RG8 Coil Accessory KitClearmri Solutions, Inc. · 2014
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −1 | K962061 | Magnetic Resonance Diagnostic System | GE Medical Systems | 1996 | 2 |
| 0 (this device) | K132381 | Clearmri Helios-RG8 Coil Accessory Kit | Clearmri Solutions, Inc. | 2014 | — |
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 LNH? 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? (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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K962061 | Magnetic Resonance Diagnostic SystemSummary page 1…lation: 21 CFR §892. 1000; Classification: II; Product Code: LNH Predicate Devices: General Electric Signa Horizon Cx Magnetic Resonance System (K962061) Device Description: The ClearMRI Solutions, Inc. Helios-ROR Coil Accessory Kit is designed as an accessory to a previously cl… | 1996 |
What descends from it?
No later submission names this one as a predicate yet.
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?
- Its one ancestor has a recall.
- 2 other devices also cite its predicate K962061.
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. 2014, this device’s year, is highlighted.
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 | — |
What is it indicated for?
The intended use of the ClearMRl Helios-R08,Coil Accessory Kit is to enable the GE Signa Horizon Cx MR System to perform MR scans of the head or body utilizing newer FDA-cleared coils (up to 8 channels), without hindering its current capability utilizing the legacy GE FDA-cleared 4-channel coils. The ClearMRl Helios-RGS Coil Accessory Kit inherits the same limitations of the GE Signa Horizon Cx MR system. The ClearMRl Helios-RG8 Coil Accessory Kit has…
Read the full statement (275 words)
The intended use of the ClearMRl Helios-R08,Coil Accessory Kit is to enable the GE Signa Horizon Cx MR System to perform MR scans of the head or body utilizing newer FDA-cleared coils (up to 8 channels), without hindering its current capability utilizing the legacy GE FDA-cleared 4-channel coils. The ClearMRl Helios-RGS Coil Accessory Kit inherits the same limitations of the GE Signa Horizon Cx MR system. The ClearMRl Helios-RG8 Coil Accessory Kit has only been validated for and is for use strictly with the GE Signa Horizon Cx MR System, software build 9.1.031 lb. The ClearMRl Helios-ROS Coil Accessory Kit allows the GE Signa Horizon Cx MR System to continue to produce transverse, sagittal, coronall and oblique images of the internal structures of the head or body with the GE Signa Horizon Cx MR System. The images produced reflect the spatial distribution of protons (hydrogen nuclei) exhibiting magnetic resonance. The NMR properties that determine the image appearance are proton density, spin lattice relaxation time (TI), spin-spin relaxation time (72) and flow. When interpreted by a trained physician, these images provide information that can be useful in determining a diagnosis.
The Helios-ROS Coil Accessory Kit will support coil anatomies from Resonance Innovations, LLC: Long Bone Array in large (model 168GEl150 1).
Accessories to medical devices arc regulated under the same classification regulation as the device(s) with which they are intended to be used. The ClearMRl Helios-ROS Coil Accessory Kit is intended to be used strictly as an accessory to the GE Signa Horizon Cx MR System, software build 9.1.0311 b, and does not change the existing indications for the GE Signa Horizon Cx MR System (K962061I).
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K132381 · printed Nov 6, 2026
Cite this page
510(k) Report. “K132381: Clearmri Helios-RG8 Coil Accessory Kit.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K132381
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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