510(k) · Cleared
ClearedActive Breathing Coordinator
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Aktina Medical Corp. · IYE Accelerator, Linear, Medical
Cleared on Aug 7, 2013 as substantially equivalent to K003330 (Aktina Medical Physics Corp., 2001) and 1 other predicate after a 92-day review. Its family tree reaches back 3 generations to 1987. 1 later device descends from it.
- Decided
- Aug 7, 2013
- Review
- 92 days
- Class
- Class II
- Product code
- IYE
- Recalls
- None
- Predicates
- 2
Its longest line of descent runs back 3 generations to K864886 (1987). 4 ancestors in all. 1 later device descends from it, 1 citing it directly.
- Root · 3 generations backK864886 Respigraph-Respisomnograph-RespicentralNims/Respitrace Corp. · 1987
- 2 generations backK983629 RPM Respiratory Gating SystemVarian Medical Systems, Inc. · 1999
- 1 generation backK031385 Anzai AZ-733 Respiratory Gating SystemAnzai Medical Co., Ltd. · 2003
- This deviceK131313 Active Breathing CoordinatorAktina Medical Corp. · 2013
- Descendant · cites it directly · 0 of its ownK151097 Active Breathing CoordinatorAktina Medical Corporation · 2015
Most influential descendants
Showing 1 of 1 · See all- K151097Active Breathing CoordinatorAktina Medical Corporation · 2015 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −3 | K864886 | Respigraph-Respisomnograph-Respicentral | Nims/Respitrace Corp. | 1987 | — |
| −2 | K983629 | RPM Respiratory Gating System | Varian Medical Systems, Inc. | 1999 | — |
| −1 | K031385 | Anzai AZ-733 Respiratory Gating System | Anzai Medical Co., Ltd. | 2003 | — |
| 0 (this device) | K131313 | Active Breathing Coordinator | Aktina Medical Corp. | 2013 | — |
| +1 | K151097 | Active Breathing Coordinator | Aktina Medical Corporation | 2015 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2001 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2015 | 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 IYE? 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 IYE device
- #1 K252977 Halcyon, Ethos Radiotherapy System (5.0)score 18.8 · 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? (2)
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 |
|---|---|---|---|
| * | K003330 | Aktina Medical Physics Corporation Active Breathing Coordinator (Abc)Summary page 1…d- particle radiation therapy system." The product code is lYE. 3. Predicate Devices 1) Active Breathing Coordinator (ABC), 510(k) No. K003330, Aktina Medical Corporation, 360 North Route 9W, Congers, NY 10920 2) Respiratory Gating System, Cat.… | 2001 |
| * | K031385 | Anzai AZ-733 Respiratory Gating SystemSummary page 1…10(k) No. K003330, Aktina Medical Corporation, 360 North Route 9W, Congers, NY 10920 2) Respiratory Gating System, Cat. No. AK-733, 510(k) No. K031385, Anzai Medical Company, Ltd., 3-6-25 Nishi-Shinagawa, Shinagawa-ku, Tokyo 14 1-0033 Japan 4. Description… | 2003 |
What descends from it? (1)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K151097 | Active Breathing Coordinator | 2015 | 0 |
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 4 companies; a new generation was cleared every 9.7 years on median.
- None of the 4 ancestors has a recall.
- Of its descendants, K151097 (Aktina Medical Corporation, 2015) has gone furthest, with 0 descendants of its own.
- 2 other devices also cite its predicate K003330.
How does its category compare?
All IYE devicesIYE Accelerator, Linear, Medical: FDA decisions, review times, recalls and adverse event reports over 20 years. 2013, this device’s year, is highlighted.
FDA decisions per year · IYE
12in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · IYE
170in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · IYE
1in 2025
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · IYE
101in 2025
MAUDE reports naming product code IYE, 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 | 23 | 44 | 78 | 155 |
| 2008 | 14 | 69 | 49 | 114 |
| 2009 | 20 | 63 | 22 | 174 |
| 2010 | 23 | 74 | 27 | 246 |
| 2011 | 11 | 94 | 73 | 280 |
| 2012 | 28 | 106 | 20 | 128 |
| 2013 | 18 | 88 | 11 | 96 |
| 2014 | 20 | 100 | 14 | 124 |
| 2015 | 20 | 108 | 8 | 100 |
| 2016 | 21 | 97 | 7 | 97 |
| 2017 | 23 | 94 | 7 | 125 |
| 2018 | 21 | 58 | 7 | 85 |
| 2019 | 19 | 83 | 2 | 91 |
| 2020 | 20 | 67 | 4 | 74 |
| 2021 | 19 | 86 | 5 | 68 |
| 2022 | 12 | 172 | 3 | 66 |
| 2023 | 18 | 129 | 7 | 128 |
| 2024 | 9 | 239 | 1 | 81 |
| 2025 | 12 | 170 | 1 | 101 |
| 2026 | 14 | 120 | 4 | — |
What is it indicated for?
The Active Breathing Coordinator is indicated for use when there is a need to reduce the anatomical movement in the thorax and abdomen caused by breathing and cardiac motion. It is intended for breath-hold (BH) during simulation and delivery of External Beam Radiation Therapy (EBRT) using photons, in single or multiple fractions, administered via static and/or dynamic delivery processes, in any and all areas of the body where such treatment is indicated.…
Read the full statement (296 words)
The Active Breathing Coordinator is indicated for use when there is a need to reduce the anatomical movement in the thorax and abdomen caused by breathing and cardiac motion. It is intended for breath-hold (BH) during simulation and delivery of External Beam Radiation Therapy (EBRT) using photons, in single or multiple fractions, administered via static and/or dynamic delivery processes, in any and all areas of the body where such treatment is indicated. It also provides electrical prompts and status information for the Elekia Limited Response TM gating interface when automated gating of the linac is used.
The Active Breathing Coordinator is specifically indicated for:
a. Breast tumors, including total and partial breast irradiation techniques, whore immobilized anatomy provided by deep inspiration breath-hold (DISH) allows critical organ sparing, such as decreasing radiation dose to heart, lung and other surrounding normal tissue.
b. Lung cancers and other thoracic tumors (such as esophagus, lymphoma, and metastatic lesions) where immobilized anatomy provided by DIBH allows critical organ spaning, including reducing both dose and volume of irradiated normal tissue, and enabling potential reduction of tumor target margins. Also included is the use of linac-based Stereotactie Radiosurgery (SRS) and Stereoitactic Radiation Therapy (SRT) that may be employed to treat such lesions.
c. Liver tumors, where immobilized anatomy provides critical organ sparing, including reducing both dose and volume of irradiated normal tissue enabling potential reduction of tumor target tissue margins. Also included is the use of linac-based SRS and SRT that may be employed to treat such lesions.
d. Pancreatic tumors, where immobilized anatomy allows critical organ sparing including reducing both dose and volume of irradiated normal tissue, enabling potential reduction of tumor target margins. Also included is the use of linac-based SRS and SRT that may be employed to treat such lesions.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K131313 · printed Nov 6, 2026
Cite this page
510(k) Report. “K131313: Active Breathing Coordinator.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K131313
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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