510(k) · Cleared
ClearedRayStation (2024A SP3)
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
RaySearch Laboratories AB (PUBL) · MUJ System, Planning, Radiation Therapy Treatment
Cleared on Dec 22, 2025 as substantially equivalent to K240398 (RaySearch Laboratories AB (PUBL), 2025) after a 168-day review. Its family tree reaches back 21 generations to 2001.
- Decided
- Dec 22, 2025
- Review
- 168 days
- Class
- Class II
- Product code
- MUJ
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 21 generations to K010975 (2001). 130 ancestors in all, the oldest K802809 (1981). No later device cites it as a predicate yet.
- Root · 21 generations backK010975 Eclipse 6.5Varian Medical Systems, Inc. · 2001 · Recalled
- 17 generations between
- 3 generations backK220141 RayStation 11BRaySearch Laboratories AB (PUBL) · 2022 · Recalled
- 2 generations backK222312 RayStation 12ARaySearch Laboratories AB (PUBL) · 2023 · Recalled
- 1 generation backK240398 RayStation 2023B, RayPlan 2023B, RayStation 2024A, RayPlan 2024A…RaySearch Laboratories AB (PUBL) · 2025 · Recalled
- This deviceK252109 RayStation (2024A SP3)RaySearch Laboratories AB (PUBL) · 2025
Show all 21 generations
- Root · 21 generations backK010975 Eclipse 6.5Varian Medical Systems, Inc. · 2001 · Recalled
- 20 generations backK030981 EclipseVarian Medical Systems, Inc. · 2003
- 19 generations backK041403 Eclipse with AaaVarian Medical Systems · 2004
- 18 generations backK050296 Eclipse Treatment Planning SystemVarian Medical Systems · 2005
- 17 generations backK071873 Modification to Eclipse Treatment Planning SystemVarian Medical Systems, Inc. · 2007 · Recalled
- 16 generations backK073020 Eclipse Treatment Planning SystemVarian Medical Systems, Inc. · 2007 · Recalled
- 15 generations backK091492 Modification to Eclipse Treatment Planning SystemVarian Medical Systems, Inc. · 2009 · Recalled
- 14 generations backK102216 Xio RTP SystemComputerized Medical Systems, Inc. · 2010 · Recalled
- 13 generations backK140187 Ray StationRaysearch Laboratories AB · 2014 · Recalled
- 12 generations backK141860 RaystationRaysearch Laboratories AB · 2014 · Recalled
- 11 generations backK160093 RayStationRaySearch Laboratories AB (PUBL) · 2016 · Recalled
- 10 generations backK170355 RayStation 6RaySearch Laboratories AB (PUBL) · 2017 · Recalled
- 9 generations backK171536 RayStationRaySearch Laboratories AB (PUBL) · 2017 · Recalled
- 8 generations backK180379 RayStation 7RaySearch Laboratories AB (PUBL) · 2018 · Recalled
- 7 generations backK190387 RayStationRaySearch Laboratories AB (PUBL) · 2019 · Recalled
- 6 generations backK200569 RayStationRaySearch Laboratories AB (PUBL) · 2020 · Recalled
- 5 generations backK210645 RayStation 10.1RaySearch Laboratories AB (PUBL) · 2021 · Recalled
- 4 generations backK211867 RayStation 11.0RaySearch Laboratories AB (PUBL) · 2021 · Recalled
- 3 generations backK220141 RayStation 11BRaySearch Laboratories AB (PUBL) · 2022 · Recalled
- 2 generations backK222312 RayStation 12ARaySearch Laboratories AB (PUBL) · 2023 · Recalled
- 1 generation backK240398 RayStation 2023B, RayPlan 2023B, RayStation 2024A, RayPlan 2024A…RaySearch Laboratories AB (PUBL) · 2025 · Recalled
- This deviceK252109 RayStation (2024A SP3)RaySearch Laboratories AB (PUBL) · 2025
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −21 | K010975 | Eclipse 6.5 | Varian Medical Systems, Inc. | 2001 | 3 |
| −20 | K030981 | Eclipse | Varian Medical Systems, Inc. | 2003 | — |
| −19 | K041403 | Eclipse with Aaa | Varian Medical Systems | 2004 | — |
| −18 | K050296 | Eclipse Treatment Planning System | Varian Medical Systems | 2005 | — |
| −17 | K071873 | Modification to Eclipse Treatment Planning System | Varian Medical Systems, Inc. | 2007 | 5 |
| −16 | K073020 | Eclipse Treatment Planning System | Varian Medical Systems, Inc. | 2007 | 6 |
| −15 | K091492 | Modification to Eclipse Treatment Planning System | Varian Medical Systems, Inc. | 2009 | 2 |
| −14 | K102216 | Xio RTP System | Computerized Medical Systems, Inc. | 2010 | 7 |
| −13 | K140187 | Ray Station | Raysearch Laboratories AB | 2014 | 1 |
| −12 | K141860 | Raystation | Raysearch Laboratories AB | 2014 | 5 |
| −11 | K160093 | RayStation | RaySearch Laboratories AB (PUBL) | 2016 | 7 |
| −10 | K170355 | RayStation 6 | RaySearch Laboratories AB (PUBL) | 2017 | 1 |
| −9 | K171536 | RayStation | RaySearch Laboratories AB (PUBL) | 2017 | 6 |
| −8 | K180379 | RayStation 7 | RaySearch Laboratories AB (PUBL) | 2018 | 7 |
| −7 | K190387 | RayStation | RaySearch Laboratories AB (PUBL) | 2019 | 32 |
| −6 | K200569 | RayStation | RaySearch Laboratories AB (PUBL) | 2020 | 14 |
| −5 | K210645 | RayStation 10.1 | RaySearch Laboratories AB (PUBL) | 2021 | 6 |
| −4 | K211867 | RayStation 11.0 | RaySearch Laboratories AB (PUBL) | 2021 | 8 |
| −3 | K220141 | RayStation 11B | RaySearch Laboratories AB (PUBL) | 2022 | 6 |
| −2 | K222312 | RayStation 12A | RaySearch Laboratories AB (PUBL) | 2023 | 6 |
| −1 | K240398 | RayStation 2023B, RayPlan 2023B, RayStation 2024A, RayPlan 2024A, RayStation… | RaySearch Laboratories AB (PUBL) | 2025 | 2 |
| 0 (this device) | K252109 | RayStation (2024A SP3) | RaySearch Laboratories AB (PUBL) | 2025 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1981 | 1 | 0 |
| 1986 | 1 | 0 |
| 1987 | 1 | 0 |
| 1989 | 3 | 0 |
| 1990 | 3 | 0 |
| 1991 | 4 | 0 |
| 1992 | 4 | 0 |
| 1993 | 1 | 0 |
| 1994 | 2 | 0 |
| 1995 | 2 | 0 |
| 1996 | 8 | 0 |
| 1997 | 4 | 0 |
| 1998 | 2 | 0 |
| 1999 | 6 | 0 |
| 2000 | 8 | 0 |
| 2001 | 10 | 0 |
| 2002 | 6 | 0 |
| 2003 | 4 | 0 |
| 2004 | 7 | 0 |
| 2005 | 3 | 0 |
| 2006 | 4 | 0 |
| 2007 | 1 | 0 |
| 2008 | 4 | 0 |
| 2009 | 2 | 0 |
| 2010 | 2 | 0 |
| 2011 | 3 | 0 |
| 2012 | 2 | 0 |
| 2013 | 2 | 0 |
| 2014 | 3 | 0 |
| 2015 | 1 | 0 |
| 2017 | 2 | 0 |
| 2018 | 2 | 0 |
| 2020 | 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 MUJ? 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 MUJ device
- #1 K232799 syngo.via RT Image Suitescore 18.6 · 19 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 |
|---|---|---|---|
| * | K240398 | RayStation 2023B, RayPlan 2023B, RayStation 2024A, RayPlan 2024A, RayStation 2024A SP3…Summary page 6…e(s) MUJ Page 1 of 10 III. Legally Marketed Predicate Device Predicate # K240398 Predicate Trade Name RayStation 2024A SP3 Product Code MUJ Reference Device used: RayStation 11B, K220141. Use of referenc… | 2025 |
| † | K220141 | RayStation 11B | 2022 |
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 24 years and passes through 5 companies; a new generation was cleared every 1.1 years on median.
- 48 of the 130 ancestors have a recall of any class.
How does its category compare?
All MUJ devicesMUJ System, Planning, Radiation Therapy Treatment: FDA decisions, review times, recalls and adverse event reports over 20 years. 2025, this device’s year, is highlighted.
FDA decisions per year · MUJ
10in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · MUJ
186in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · MUJ
2in 2023
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · MUJ
21in 2025
MAUDE reports naming product code MUJ, 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 | 67 | 4 | 24 |
| 2008 | 9 | 63 | 10 | 51 |
| 2009 | 16 | 84 | 11 | 24 |
| 2010 | 11 | 56 | 23 | 78 |
| 2011 | 9 | 103 | 17 | 73 |
| 2012 | 8 | 59 | 4 | 39 |
| 2013 | 5 | 64 | 6 | 33 |
| 2014 | 9 | 108 | 2 | 35 |
| 2015 | 13 | 78 | 7 | 30 |
| 2016 | 5 | 80 | 13 | 27 |
| 2017 | 7 | 30 | 4 | 16 |
| 2018 | 7 | 53 | 3 | 25 |
| 2019 | 9 | 56 | 4 | 25 |
| 2020 | 9 | 104 | 2 | 26 |
| 2021 | 11 | 87 | 4 | 15 |
| 2022 | 8 | 168 | 3 | 22 |
| 2023 | 10 | 140 | 2 | 76 |
| 2024 | 9 | 122 | 0 | 9 |
| 2025 | 10 | 186 | 0 | 21 |
| 2026 | 9 | 233 | 2 | — |
What is it indicated for?
RayStation is a software system for radiation therapy and medical oncology. Based on user input, RayStation proposes treatment plans. After a proposed treatment plan is reviewed and approved by authorized intended users, RayStation may also be used to administer treatments.
The system functionality can be configured based on user needs.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K252109 · printed Nov 6, 2026
Cite this page
510(k) Report. “K252109: RayStation (2024A SP3).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K252109
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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