510(k) · Cleared
ClearedThe Coeur Injector Adaptor/Pressure Jacket, Model C859-6003
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Coeur Medical · DXT Injector And Syringe, Angiographic
Cleared on Dec 16, 2003 after an 85-day review. FDA’s file for it is a 510(k) statement, which names no predicate. 3 later devices descend from it.
- Decided
- Dec 16, 2003
- Review
- 85 days
- Class
- Class II
- Product code
- DXT
- Recalls
- None
- Predicates
- 0
3 later devices descend from it, 1 citing it directly.
- This deviceK032920 The Coeur Injector Adaptor/Pressure Jacket, Model C859-6003Coeur Medical · 2003
- Descendant · cites it directly · 2 of its ownK070798 Adapters for CT, Angiographic, and/or Mri Power InjectorsCoeur, Inc. · 2007
- Descendant · 2 generations on · 0 of its ownK170431 CT Syringe for Stellant Injectors (with & without Spikes, Prime…Coeur, Inc. · 2017
- Descendant · 2 generations on · 0 of its ownK133600 Coeur, Inc. Frontload for Optivantage Power InjectorCoeur, Inc. · 2014
Most influential descendants
Showing 3 of 3 · See all- K070798Adapters for CT, Angiographic, and/or Mri Power InjectorsCoeur, Inc. · 2007 · cites it directly2descendants
- K170431CT Syringe for Stellant Injectors (with & without Spikes, Prime Tubes, & Fill Tubes), CT…Coeur, Inc. · 2017 · 2 generations on0descendants
- K133600Coeur, Inc. Frontload for Optivantage Power InjectorCoeur, Inc. · 2014 · 2 generations on0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| 0 (this device) | K032920 | The Coeur Injector Adaptor/Pressure Jacket, Model C859-6003 | Coeur Medical | 2003 | — |
| +1 | K070798 | Adapters for CT, Angiographic, and/or Mri Power Injectors | Coeur, Inc. | 2007 | — |
| +2 | K170431 | CT Syringe for Stellant Injectors (with & without Spikes, Prime Tubes, & Fill… | Coeur, Inc. | 2017 | — |
| +2 | K133600 | Coeur, Inc. Frontload for Optivantage Power Injector | Coeur, Inc. | 2014 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2007 | 1 | 0 |
| 2014 | 1 | 0 |
| 2017 | 1 | 0 |
Sources: FDA 510(k) database (decision fields), the FDA 510(k) statement (indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
Planning a device in DXT? 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 DXT device
- #1 K253048 High Pressure Syringe; Pressure Connecting…score 13.6 · 9 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’s file for it is a 510(k) statement, which names no predicate.
What descends from it? (3)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K070798 | Adapters for CT, Angiographic, and/or Mri Power Injectors | 2007 | 2 |
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?
- Of its descendants, K070798 (Coeur, Inc., 2007) has gone furthest, with 2 descendants of its own.
How does its category compare?
All DXT devicesDXT Injector And Syringe, Angiographic: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · DXT
1in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · DXT
138in 2024
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · DXT
10in 2024
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · DXT
97in 2025
MAUDE reports naming product code DXT, 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 | 3 | 182 | 4 | 107 |
| 2008 | 2 | — | 3 | 168 |
| 2009 | 6 | 137 | 7 | 188 |
| 2010 | 1 | — | 3 | 124 |
| 2011 | 4 | 69 | 3 | 133 |
| 2012 | 0 | — | 7 | 135 |
| 2013 | 2 | — | 0 | 141 |
| 2014 | 6 | 144 | 0 | 97 |
| 2015 | 7 | 153 | 1 | 135 |
| 2016 | 8 | 172 | 0 | 152 |
| 2017 | 7 | 183 | 0 | 128 |
| 2018 | 9 | 93 | 2 | 129 |
| 2019 | 4 | 96 | 0 | 121 |
| 2020 | 3 | 154 | 1 | 93 |
| 2021 | 1 | — | 1 | 132 |
| 2022 | 0 | — | 0 | 111 |
| 2023 | 1 | — | 2 | 117 |
| 2024 | 4 | 138 | 10 | 118 |
| 2025 | 1 | — | 0 | 97 |
| 2026 | 7 | 264 | 6 | — |
What is it indicated for?
The Coeur Injector Adaptor / Pressure Jacket is intended to be installed on Liebel-Flarsheim Angiomat 6000 and Angiomat Illumena Contrast Delivery Systems to allow the injectors to be used with the Coeur 150mL A-Series (Angiographic and CT) Syringes (Catalog Numbers: C853-6150 and C853-6159).
Indications for use as stated in the FDA 510(k) statement.
https://510kreport.com/device/K032920 · printed Nov 6, 2026
Cite this page
510(k) Report. “K032920: The Coeur Injector Adaptor/Pressure Jacket, Model C859-6003.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K032920
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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