510(k) · Cleared
ClearedTheraplan Plus Version 1.2
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Theratronics, Inc. · IYE Accelerator, Linear, Medical
Cleared on Jul 9, 1997 as substantially equivalent to K954679 (Theratronics, Inc., 1996) and 5 other predicates after a 169-day review. Its family tree reaches back 1 generation to 1987. 65 later devices descend from it.
- Decided
- Jul 9, 1997
- Review
- 169 days
- Class
- Class II
- Product code
- IYE
- Recalls
- None
- Predicates
- 6
Its longest line of descent runs back 1 generation to K862643 (1987). 6 ancestors in all. 65 later devices descend from it, 3 citing it directly.
- Root · 1 generation backK862643 Radiation Oncology Computer Sys Treatment PlanningPacific Physics, Inc. · 1987
- This deviceK970236 Theraplan Plus Version 1.2Theratronics, Inc. · 1997
- Descendant · cites it directly · 59 of its ownK031349 OTP 1.2Nucletron Corp. · 2003
- Descendant · 2 generations on · 54 of its ownK081281 Ocentra Masterplan 3.1 (Ocentra Brachy)Nucletron Corporation · 2008 · Recalled
- Descendant · 3 generations on · 34 of its ownK092132 Xio RTP SystemComputerized Medical Systems, Inc. · 2009 · Recalled
- Descendant · 3 generations on · 31 of its ownK083264 Rayautoplan 1.0Raysearch Laboratories AB · 2009 · Recalled
- Descendant · 3 generations on · 30 of its ownK100552 Raystation Version 1.0Raysearch Laboratories AB · 2010 · Recalled
Showing 5 of 65 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 65 · See all- K031349OTP 1.2Nucletron Corp. · 2003 · cites it directly59descendants
- K081281Ocentra Masterplan 3.1 (Ocentra Brachy)Nucletron Corporation · 2008 · 2 generations on54descendants
- K092132Xio RTP SystemComputerized Medical Systems, Inc. · 2009 · 3 generations on34descendants
- K083264Rayautoplan 1.0Raysearch Laboratories AB · 2009 · 3 generations on31descendants
- K100552Raystation Version 1.0Raysearch Laboratories AB · 2010 · 3 generations on30descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −1 | K862643 | Radiation Oncology Computer Sys Treatment Planning | Pacific Physics, Inc. | 1987 | — |
| 0 (this device) | K970236 | Theraplan Plus Version 1.2 | Theratronics, Inc. | 1997 | — |
| +1 | K031349 | OTP 1.2 | Nucletron Corp. | 2003 | — |
| +2 | K081281 | Ocentra Masterplan 3.1 (Ocentra Brachy) | Nucletron Corporation | 2008 | 2 |
| +3 | K092132 | Xio RTP System | Computerized Medical Systems, Inc. | 2009 | 12 |
| +3 | K083264 | Rayautoplan 1.0 | Raysearch Laboratories AB | 2009 | 2 |
| +3 | K100552 | Raystation Version 1.0 | Raysearch Laboratories AB | 2010 | 4 |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1990 | 1 | 0 |
| 1992 | 1 | 0 |
| 1994 | 2 | 0 |
| 1996 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1998 | 2 | 0 |
| 1999 | 1 | 0 |
| 2000 | 1 | 0 |
| 2003 | 2 | 0 |
| 2007 | 1 | 0 |
| 2008 | 2 | 0 |
| 2009 | 3 | 0 |
| 2010 | 4 | 0 |
| 2011 | 1 | 0 |
| 2012 | 3 | 0 |
| 2013 | 3 | 0 |
| 2014 | 4 | 0 |
| 2015 | 3 | 0 |
| 2016 | 3 | 0 |
| 2017 | 5 | 0 |
| 2018 | 5 | 0 |
| 2019 | 4 | 0 |
| 2020 | 3 | 0 |
| 2021 | 3 | 0 |
| 2022 | 4 | 0 |
| 2023 | 3 | 0 |
| 2024 | 2 | 0 |
| 2025 | 2 | 0 |
| 2026 | 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? (6)
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 |
|---|---|---|---|
| * | K954679 | Theraplan PlusSummary page 1…AN Plus Version 1.2 Common Name: Radiation Therapy Treatment Planning System Classification Name: Treatment Planning Computer Theratronics “THERAPLAN PLUS Version 1.0”, K954679 Theratronics "THERAPLAN 500", K940237 Nucletron "PLATO", K921991 Radiation Oncology Computer Systems "TPS 1031", K862643 Precis… | 1996 |
| * | K940237 | Theraplan V05B/ TP-11 V09BSummary page 1…tion Therapy Treatment Planning System Classification Name: Treatment Planning Computer Theratronics “THERAPLAN PLUS Version 1.0”, K954679 Theratronics "THERAPLAN 500", K940237 Nucletron "PLATO", K921991 Radiation Oncology Computer Systems "TPS 1031", K862643 Precision Therapy "Render-Plan", K894722 AD… | 1994 |
| * | K921991 | Plato Radiation Therapy Planning SystemSummary page 1…ing System Classification Name: Treatment Planning Computer Theratronics “THERAPLAN PLUS Version 1.0”, K954679 Theratronics "THERAPLAN 500", K940237 Nucletron "PLATO", K921991 Radiation Oncology Computer Systems "TPS 1031", K862643 Precision Therapy "Render-Plan", K894722 ADAC "Pinnacle", K926008 N A… | 1992 |
| * | K862643 | Radiation Oncology Computer Sys Treatment PlanningSummary page 1…er Theratronics “THERAPLAN PLUS Version 1.0”, K954679 Theratronics "THERAPLAN 500", K940237 Nucletron "PLATO", K921991 Radiation Oncology Computer Systems "TPS 1031", K862643 Precision Therapy "Render-Plan", K894722 ADAC "Pinnacle", K926008 N A THERAPLAN Plus Version 1.2 consists principally of appli… | 1987 |
| * | K894722 | Renner-PlanSummary page 1…1.0”, K954679 Theratronics "THERAPLAN 500", K940237 Nucletron "PLATO", K921991 Radiation Oncology Computer Systems "TPS 1031", K862643 Precision Therapy "Render-Plan", K894722 ADAC "Pinnacle", K926008 N A THERAPLAN Plus Version 1.2 consists principally of application software running under a Windows o… | 1990 |
| * | K926008 | Pinnacle 3Summary page 1…"THERAPLAN 500", K940237 Nucletron "PLATO", K921991 Radiation Oncology Computer Systems "TPS 1031", K862643 Precision Therapy "Render-Plan", K894722 ADAC "Pinnacle", K926008 N A THERAPLAN Plus Version 1.2 consists principally of application software running under a Windows operating system on a Penti… | 1994 |
What descends from it? (65)
See all 653 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?
- None of the 6 ancestors has a recall.
- Of its descendants, K031349 (Nucletron Corp., 2003) has gone furthest, with 59 descendants of its own.
How does its category compare?
All IYE devicesIYE Accelerator, Linear, Medical: FDA decisions, review times, recalls and adverse event reports over 20 years.
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?
THERAPLAN Plus Version 1.2 is intended to be used as a modelling system to assist health care professionals determine a course of Radiation Therapy to be delivered to a patient with cancer. It is designed to be used directly by a health care professional capable of assessing the suitability of the output for treatment planning purposes, or to have its output reviewed by someone with these qualifications prior to use.
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/K970236 · printed Nov 4, 2026
Cite this page
510(k) Report. “K970236: Theraplan Plus Version 1.2.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K970236
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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