510(k) · Cleared
ClearedTerumo Capiox FX15 and FX25 Hollow Fiber Oxygenator/Reservoir
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Terumo Cardiovascular Systems Corporation · DTZ Oxygenator, Cardiopulmonary Bypass
Cleared on Jun 2, 2014 as substantially equivalent to K071494 (Terumo Corp., 2007) and 2 other predicates after a 66-day review. Its family tree reaches back 7 generations to 1992. 5 later devices descend from it.
- Decided
- Jun 2, 2014
- Review
- 66 days
- Class
- Class II
- Product code
- DTZ
- Recalls
- None
- Predicates
- 3
Its longest line of descent runs back 7 generations to K915573 (1992). 19 ancestors in all, the oldest K842908 (1985). 5 later devices descend from it, 2 citing it directly.
- Root · 7 generations backK915573 Venous Reservoir W/Cardiotomy FilterBaxter Healthcare Corp · 1992
- 6 generations backK982223 Capiox SX Hardshell ResevoirTerumo Medical Corp. · 1998
- 5 generations backK991973 Capiox SX10 Hardshell ResevoirTerumo Medical Corp. · 1999
- 4 generations backK030449 Modification to Capiox SX10 Hardshell ReservoirTerumo Corp. · 2003
- 3 generations backK051997 Capiox RX15 Hollow, Fiber Oxygenator with/Without Hardshell ReservoirTerumo Cardiovascular Systems Corp. · 2005 · Recalled
- 2 generations backK071494 Capiox FX15 and FX25 Hollow Fiber Oxygenator and Arterial FilterTerumo Corp. · 2007 · Recalled
- 1 generation backK130520 Capiox FX15 and FX25 Hollow Fiber Oxygenator/ReservoirAshitaka Factory of Terumo Corp. · 2013
- This deviceK140774 Terumo Capiox FX15 and FX25 Hollow Fiber Oxygenator/ReservoirTerumo Cardiovascular Systems Corporation · 2014
- Descendant · cites it directly · 2 of its ownK151791 Terumo Capiox FX15 Advance Oxygenator with Integrated Arterial…Terumo Cardiovascular Systems Corporation · 2015 · Recalled
- Descendant · cites it directly · 1 of its ownK151389 Terumo Capiox FX15 Advance Oxygenator with Integrated Arterial…Terumo Cardiovascular Systems Corporation · 2015
- Descendant · 2 generations on · 0 of its ownK242503 Trilly Pediatric Oxygenator with Integrated Arterial Filter (US5232)Eurosets S.R.L · 2025
- Descendant · 2 generations on · 0 of its ownK180950 Terumo Capiox NX19 Oxygenator with Reservoir (east Orientation)…Terumo Cardiovascular Systems Corporation · 2018 · Recalled
- Descendant · 2 generations on · 0 of its ownK172071 Terumo Capiox NX19 Oxygenator with Reservoir (east orientation )…Terumo Cardiovascular Systems Corporation · 2018
Most influential descendants
Showing 5 of 5 · See all- K151791Terumo Capiox FX15 Advance Oxygenator with Integrated Arterial Filter and Reservoir…Terumo Cardiovascular Systems Corporation · 2015 · cites it directly2descendants
- K151389Terumo Capiox FX15 Advance Oxygenator with Integrated Arterial Filter and Hardshell…Terumo Cardiovascular Systems Corporation · 2015 · cites it directly1descendant
- K242503Trilly Pediatric Oxygenator with Integrated Arterial Filter (US5232)Eurosets S.R.L · 2025 · 2 generations on0descendants
- K180950Terumo Capiox NX19 Oxygenator with Reservoir (east Orientation), Terumo Capiox NX19…Terumo Cardiovascular Systems Corporation · 2018 · 2 generations on0descendants
- K172071Terumo Capiox NX19 Oxygenator with Reservoir (east orientation ), Terumo Capiox NX19…Terumo Cardiovascular Systems Corporation · 2018 · 2 generations on0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −7 | K915573 | Venous Reservoir W/Cardiotomy Filter | Baxter Healthcare Corp | 1992 | — |
| −6 | K982223 | Capiox SX Hardshell Resevoir | Terumo Medical Corp. | 1998 | — |
| −5 | K991973 | Capiox SX10 Hardshell Resevoir | Terumo Medical Corp. | 1999 | — |
| −4 | K030449 | Modification to Capiox SX10 Hardshell Reservoir | Terumo Corp. | 2003 | — |
| −3 | K051997 | Capiox RX15 Hollow, Fiber Oxygenator with/Without Hardshell Reservoir | Terumo Cardiovascular Systems Corp. | 2005 | 1 |
| −2 | K071494 | Capiox FX15 and FX25 Hollow Fiber Oxygenator and Arterial Filter | Terumo Corp. | 2007 | 12 |
| −1 | K130520 | Capiox FX15 and FX25 Hollow Fiber Oxygenator/Reservoir | Ashitaka Factory of Terumo Corp. | 2013 | — |
| 0 (this device) | K140774 | Terumo Capiox FX15 and FX25 Hollow Fiber Oxygenator/Reservoir | Terumo Cardiovascular Systems Corporation | 2014 | — |
| +1 | K151791 | Terumo Capiox FX15 Advance Oxygenator with Integrated Arterial Filter and… | Terumo Cardiovascular Systems Corporation | 2015 | 2 |
| +1 | K151389 | Terumo Capiox FX15 Advance Oxygenator with Integrated Arterial Filter and… | Terumo Cardiovascular Systems Corporation | 2015 | — |
| +2 | K242503 | Trilly Pediatric Oxygenator with Integrated Arterial Filter (US5232) | Eurosets S.R.L | 2025 | — |
| +2 | K180950 | Terumo Capiox NX19 Oxygenator with Reservoir (east Orientation), Terumo Capiox… | Terumo Cardiovascular Systems Corporation | 2018 | 5 |
| +2 | K172071 | Terumo Capiox NX19 Oxygenator with Reservoir (east orientation ), Terumo… | Terumo Cardiovascular Systems Corporation | 2018 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1985 | 1 | 0 |
| 1994 | 1 | 0 |
| 1996 | 2 | 0 |
| 1998 | 1 | 0 |
| 2000 | 2 | 0 |
| 2002 | 1 | 0 |
| 2004 | 1 | 0 |
| 2005 | 1 | 0 |
| 2006 | 1 | 0 |
| 2013 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2015 | 2 | 0 |
| 2018 | 2 | 0 |
| 2025 | 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 DTZ? 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 DTZ device
- #1 K240934 Quantum Perfusion Blood Oxygenator ECC…score 14.3 · 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? (3)
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 |
|---|---|---|---|
| * | K071494 | Capiox FX15 and FX25 Hollow Fiber Oxygenator and Arterial FilterSummary page 2…n intended use, design, technology/principles of operation, materials and specifications to thle following devices: * Terumno®CAPIOX FX 15 and FX25 Oxygenator/Reservoir -K07 1494 " Terumo® CAP1OXO~FX IS and FX25 Oxygenator/Reservoir -K 130520 * TerumoWo CAPIOX' RX 15 and, RX25 Oxygenator/Reservoir - K130333… | 2007 |
| * | K130520 | Capiox FX15 and FX25 Hollow Fiber Oxygenator/ReservoirSummary page 2…rials and specifications to thle following devices: * Terumno®CAPIOX FX 15 and FX25 Oxygenator/Reservoir -K07 1494 " Terumo® CAP1OXO~FX IS and FX25 Oxygenator/Reservoir -K 130520 * TerumoWo CAPIOX' RX 15 and, RX25 Oxygenator/Reservoir - K130333… | 2013 |
| * | K130333 | Capix RX Hollow Fiber Oxygenator with/Without Hardshell ReservoirSummary page 2…X FX 15 and FX25 Oxygenator/Reservoir -K07 1494 " Terumo® CAP1OXO~FX IS and FX25 Oxygenator/Reservoir -K 130520 * TerumoWo CAPIOX' RX 15 and, RX25 Oxygenator/Reservoir - K130333 37… | 2013 |
What descends from it? (5)
2 later devices cite it directly; ranked here by how many devices descend from each in turn.
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 22 years and passes through 6 companies; a new generation was cleared every 2.5 years on median.
- 4 of the 19 ancestors have a recall of any class.
- Of its descendants, K151791 (Terumo Cardiovascular Systems Corporation, 2015) has gone furthest, with 2 descendants of its own.
- 1 other device also cites its predicate K071494.
How does its category compare?
All DTZ devicesDTZ Oxygenator, Cardiopulmonary Bypass: FDA decisions, review times, recalls and adverse event reports over 20 years. 2014, this device’s year, is highlighted.
FDA decisions per year · DTZ
2in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · DTZ
124in 2024
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · DTZ
1in 2025
Class I (3 since 2007) Class II/III not classified
Adverse event reports per year · DTZ
976in 2025
MAUDE reports naming product code DTZ, 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 | 4 | 55 | 7 | 134 |
| 2008 | 3 | 88 | 5 | 105 |
| 2009 | 9 | 210 | 0 | 52 |
| 2010 | 2 | — | 1 | 119 |
| 2011 | 4 | 160 | 13 | 190 |
| 2012 | 9 | 90 | 14 | 215 |
| 2013 | 9 | 28 | 0 | 346 |
| 2014 | 5 | 28 | 2 | 764 |
| 2015 | 9 | 134 | 0 | 658 |
| 2016 | 3 | 62 | 1 | 443 |
| 2017 | 2 | — | 0 | 388 |
| 2018 | 3 | 72 | 2 (2) | 320 |
| 2019 | 5 | 90 | 1 | 489 |
| 2020 | 5 | 93 | 3 | 442 |
| 2021 | 5 | 336 | 1 (1) | 595 |
| 2022 | 2 | — | 6 | 559 |
| 2023 | 5 | 145 | 0 | 738 |
| 2024 | 3 | 124 | 0 | 535 |
| 2025 | 2 | — | 1 | 976 |
| 2026 | 3 | 137 | 0 | — |
What is it indicated for?
The Capiox FX Hollow Fiber Oxygenator and Arterial Filter is intended to be used to exchange gases between blood and a gaseous environment to satisfy the gas exchange needs of a patient during cardiopulmonary bypass surgery. The integrated arterial filter Is Intended to filtrate non-biologic particles and entoll and to facilitate air bubble removal from the blood flowing through the cardiopulmonary bypass circuit. The integrated heat exchanger is wsed to…
Read the full statement (242 words)
The Capiox FX Hollow Fiber Oxygenator and Arterial Filter is intended to be used to exchange gases between blood and a gaseous environment to satisfy the gas exchange needs of a patient during cardiopulmonary bypass surgery.
The integrated arterial filter Is Intended to filtrate non-biologic particles and entoll and to facilitate air bubble removal from the blood flowing through the cardiopulmonary bypass circuit.
The integrated heat exchanger is wsed to warm or cool blood and/or perfusion fluid as it flows through the device.
The hardshell reservoir is used to store blood during extra-corporeal circulation from -the venous line and the cardiotomy line. The reservoir contains a venous section that is comprised of a filter and deframer to facilitate air bubble removal. The cardiotomy section of the reservoir contains a filter to remove particulate matter and a det'oamer to facilitate air bubble removal. The 3-iter and 4-liter reservoirs may be used fur Vacuum Assisted Drainage procedures and Post Operative Chest Drainage Procedures.
The Cap lox P1X15 is fbr use with patients when the required blood flow rate will not exceed 5.0 L/min. when used with a 4 Liter Reservoir; and when the required blood flow rate will not exceed 4.0 L/nin. when used with a 3 Liter Reservoir.
The Capiox PX2S is for use with patients when the required blood flow rate will not exceed 7.0 L/min.
Theo Capiox FX Oxygenator/Reservoir/Arterial Filter assemblies can be used in procedures lasting up to 6 hours.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K140774 · printed Nov 4, 2026
Cite this page
510(k) Report. “K140774: Terumo Capiox FX15 and FX25 Hollow Fiber Oxygenator/Reservoir.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K140774
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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