510(k) · Cleared
ClearedECG CT Gating Device
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Neocoil, LLC · JAK System, X-Ray, Tomography, Computed
Cleared on Jun 16, 2016 as substantially equivalent to K991766 (Toshiba America Medical Systems, In.C, 1999) after a 129-day review. Its family tree reaches back 4 generations to 1990.
- Decided
- Jun 16, 2016
- Review
- 129 days
- Class
- Class II
- Product code
- JAK
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 4 generations to K903701 (1990). No later device cites it as a predicate yet.
- Root · 4 generations backK903701 XpressToshiba America Medical Systems, In.C · 1990
- 3 generations backK982265 Aquilion CT Scanner, Model TSX-101AToshiba America Medical Systems, In.C · 1998 · Recalled
- 2 generations backK990134 Multislice Upgrade Kit for Aquilion CT Scanner, TSX-101A…Toshiba America Medical Systems, In.C · 1999
- 1 generation backK991766 Ecg-Gating System for Aquilion CT Scanner, TSX-101AToshiba America Medical Systems, In.C · 1999
- This deviceK160350 ECG CT Gating DeviceNeocoil, LLC · 2016
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −4 | K903701 | Xpress | Toshiba America Medical Systems, In.C | 1990 | — |
| −3 | K982265 | Aquilion CT Scanner, Model TSX-101A | Toshiba America Medical Systems, In.C | 1998 | 3 |
| −2 | K990134 | Multislice Upgrade Kit for Aquilion CT Scanner, TSX-101A (Aquilion,Multi) | Toshiba America Medical Systems, In.C | 1999 | — |
| −1 | K991766 | Ecg-Gating System for Aquilion CT Scanner, TSX-101A | Toshiba America Medical Systems, In.C | 1999 | — |
| 0 (this device) | K160350 | ECG CT Gating Device | Neocoil, LLC | 2016 | — |
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 JAK? 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 JAK device
- #1 K230223 iCAC Devicescore 23.5 · 12 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 |
|---|---|---|---|
| * | K991766 | Ecg-Gating System for Aquilion CT Scanner, TSX-101ASummary page 4…patible with Toshiba Aquilion ONE and Aquilion PRIME CT scanners. 5.7. Predicate Device • ECG-Gating System for Aquilion CT Scanner, TSX-101A, K991766 as cleared on 08/10/1999. 2016 NeoCoil, LLC K160350 NeoCoil ECG CT Gating Device… | 1999 |
| † | K110987 | Cardiac Trigger Monitor | 2011 |
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?
- The line of descent spans 26 years and passes through 2 companies; a new generation was cleared every 7.8 years on median.
- 1 of the 4 ancestors has a recall of any class.
How does its category compare?
All JAK devicesJAK System, X-Ray, Tomography, Computed: FDA decisions, review times, recalls and adverse event reports over 20 years. 2016, this device’s year, is highlighted.
FDA decisions per year · JAK
27in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · JAK
141in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · JAK
17in 2025
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · JAK
219in 2025
MAUDE reports naming product code JAK, 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 | 14 | 27 | 11 | 76 |
| 2008 | 26 | 42 | 16 | 120 |
| 2009 | 15 | 31 | 29 | 105 |
| 2010 | 7 | 92 | 51 | 119 |
| 2011 | 16 | 155 | 34 | 205 |
| 2012 | 28 | 121 | 23 | 192 |
| 2013 | 17 | 132 | 11 | 414 |
| 2014 | 30 | 200 | 10 | 308 |
| 2015 | 30 | 140 | 28 | 454 |
| 2016 | 25 | 129 | 44 | 365 |
| 2017 | 29 | 96 | 33 | 338 |
| 2018 | 24 | 114 | 10 | 543 |
| 2019 | 28 | 94 | 5 | 233 |
| 2020 | 30 | 112 | 8 | 177 |
| 2021 | 20 | 145 | 15 | 261 |
| 2022 | 30 | 131 | 9 | 199 |
| 2023 | 27 | 139 | 9 | 310 |
| 2024 | 26 | 141 | 20 | 212 |
| 2025 | 27 | 141 | 17 | 219 |
| 2026 | 21 | 167 | 23 | — |
What is it indicated for?
To be used in conjunction with a CT scanner to acquire gated cardiac images. The product is an aid to the acquisition of CT cardiac scans.
Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.
https://510kreport.com/device/K160350 · printed Nov 6, 2026
Cite this page
510(k) Report. “K160350: ECG CT Gating Device.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K160350
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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