510(k) · Cleared
ClearedCaregraph
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Siemens Medical Solutions USA, Inc. · JAA System, X-Ray, Fluoroscopic, Image-Intensified
Cleared on Sep 22, 1998 as substantially equivalent to K853753 (Victoreen, Inc., 1985) after an 82-day review. Its family tree reaches back 1 generation to 1985. 10 later devices descend from it.
- Decided
- Sep 22, 1998
- Review
- 82 days
- Class
- Class II
- Product code
- JAA
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 1 generation to K853753 (1985). 10 later devices descend from it, 1 citing it directly.
- Root · 1 generation backK853753 Diamentor Patient X-Ray Exposure Indicator 07302Victoreen, Inc. · 1985
- This deviceK982319 CaregraphSiemens Medical Solutions USA, Inc. · 1998
- Descendant · cites it directly · 9 of its ownK123097 Dose Tracking System Model Xidf-DTS801Toshiba America Medical Systems, In.C · 2013
- Descendant · 2 generations on · 8 of its ownK132106 Infinix Angio Workstation W/DTS SoftwareToshiba America Medical Systems, In.C · 2013
- Descendant · 3 generations on · 7 of its ownK141541 Xidf-AWS801, Angio Workstation, V5.31Toshibamedical Systems Corporation · 2014
- Descendant · 4 generations on · 6 of its ownK142736 XIDF-AWS801, Angio Workstation, v5.31Toshibamedical Systems Corporation · 2015
- Descendant · 5 generations on · 5 of its ownK150967 XIDF-AWS801, Angio Workstation, V6.10Toshibamedical Systems Corporation · 2015 · Recalled
Showing 5 of 10 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 10 · See all- K123097Dose Tracking System Model Xidf-DTS801Toshiba America Medical Systems, In.C · 2013 · cites it directly9descendants
- K132106Infinix Angio Workstation W/DTS SoftwareToshiba America Medical Systems, In.C · 2013 · 2 generations on8descendants
- K141541Xidf-AWS801, Angio Workstation, V5.31Toshibamedical Systems Corporation · 2014 · 3 generations on7descendants
- K142736XIDF-AWS801, Angio Workstation, v5.31Toshibamedical Systems Corporation · 2015 · 4 generations on6descendants
- K150967XIDF-AWS801, Angio Workstation, V6.10Toshibamedical Systems Corporation · 2015 · 5 generations on5descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −1 | K853753 | Diamentor Patient X-Ray Exposure Indicator 07302 | Victoreen, Inc. | 1985 | — |
| 0 (this device) | K982319 | Caregraph | Siemens Medical Solutions USA, Inc. | 1998 | — |
| +1 | K123097 | Dose Tracking System Model Xidf-DTS801 | Toshiba America Medical Systems, In.C | 2013 | — |
| +2 | K132106 | Infinix Angio Workstation W/DTS Software | Toshiba America Medical Systems, In.C | 2013 | — |
| +3 | K141541 | Xidf-AWS801, Angio Workstation, V5.31 | Toshibamedical Systems Corporation | 2014 | — |
| +4 | K142736 | XIDF-AWS801, Angio Workstation, v5.31 | Toshibamedical Systems Corporation | 2015 | — |
| +5 | K150967 | XIDF-AWS801, Angio Workstation, V6.10 | Toshibamedical Systems Corporation | 2015 | 1 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2013 | 2 | 0 |
| 2014 | 1 | 0 |
| 2015 | 3 | 0 |
| 2017 | 1 | 0 |
| 2018 | 1 | 0 |
| 2022 | 1 | 0 |
| 2023 | 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 JAA? 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 JAA device
- #1 K253103 Nexus DRF Digital X-ray Imaging Systemscore 13.2 · 7 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 |
|---|---|---|---|
| * | K853753 | Diamentor Patient X-Ray Exposure Indicator 07302Summary page 1…and Image Intensified Fluoroscopic X-ray Systems currently in commercial distribution. Device Manufacturer 510(k) Number Diamentor patient Manufacturer: PTW - Freiburg K853753 x-ray exposure indicator Importer: Nuclear Associates Diamentor M1/M2/M3 Manufacturer: PTW - Freiburg exempt Simplified 510(k… | 1985 |
| * | — | Diamentor M1/M2/M3 Named without a submission number |
What descends from it? (10)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K123097 | Dose Tracking System Model Xidf-DTS801 | 2013 | 9 |
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?
- Its one ancestor has no recall.
- Of its descendants, K123097 (Toshiba America Medical Systems, In.C, 2013) has gone furthest, with 9 descendants of its own.
How does its category compare?
All JAA devicesJAA System, X-Ray, Fluoroscopic, Image-Intensified: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · JAA
2in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · JAA
89in 2024
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · JAA
4in 2025
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · JAA
33in 2025
MAUDE reports naming product code JAA, 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 | 1 | — | 35 | 9,517 |
| 2008 | 6 | 18 | 21 | 9,484 |
| 2009 | 0 | — | 18 | 12,040 |
| 2010 | 1 | — | 6 | 5,803 |
| 2011 | 4 | 48 | 7 | 14,000 |
| 2012 | 1 | — | 2 | 11,684 |
| 2013 | 6 | 129 | 3 | 13,706 |
| 2014 | 6 | 276 | 1 | 10,265 |
| 2015 | 3 | 197 | 1 | 2,922 |
| 2016 | 2 | — | 7 | 35 |
| 2017 | 1 | — | 3 | 56 |
| 2018 | 3 | 30 | 1 | 36 |
| 2019 | 6 | 49 | 2 | 49 |
| 2020 | 4 | 39 | 2 | 39 |
| 2021 | 6 | 104 | 2 | 35 |
| 2022 | 1 | — | 5 | 34 |
| 2023 | 2 | — | 9 | 41 |
| 2024 | 3 | 89 | 2 | 25 |
| 2025 | 2 | — | 4 | 33 |
| 2026 | 1 | — | 0 | — |
What is it indicated for?
CAREGRAPH is an angiographic system accessory for recording, displaying and documenting the regional distribution of the skin entry dose of a patient, depending on the relevant angulations in X-ray examination. The dose is calculated depending on the format size, the angulation and the table position and displayed on a graphical patient body surface.
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/K982319 · printed Nov 4, 2026
Cite this page
510(k) Report. “K982319: Caregraph.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K982319
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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