510(k) · Cleared
ClearedArterys Viewer
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Arterys, Inc. · LLZ System, Image Processing, Radiological
Cleared on Jul 18, 2017 as substantially equivalent to K152186 (Healthmyne, Inc., 2015) after a 53-day review. Its family tree reaches back 4 generations to 1993. 6 later devices descend from it.
- Decided
- Jul 18, 2017
- Review
- 53 days
- Class
- Class II
- Product code
- LLZ
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 4 generations to K922164 (1993). 8 ancestors in all, the oldest K920319 (1992). 6 later devices descend from it, 2 citing it directly.
- Root · 4 generations backK922164 Raytel Digital Imaging SystemsOlicon Imaging Systems, Inc. · 1993
- 3 generations backK973959 Olicon Imaging Systems, Inc. 02-Workstation and/or Pacsview SoftwareOlicon Imaging Systems, Inc. · 1997
- 2 generations backK043146 Horizon Medical ImagingMckesson Medical Imaging Company · 2005 · Recalled
- 1 generation backK152186 HealthMyne PACSHealthmyne, Inc. · 2015
- This deviceK171544 Arterys ViewerArterys, Inc. · 2017
- Descendant · cites it directly · 3 of its ownK182034 Arterys MICAArterys, Inc. · 2018
- Descendant · 2 generations on · 2 of its ownK192437 Arterys MICAArterys, Inc. · 2020
- Descendant · 3 generations on · 1 of its ownK203744 Arterys MICAArterys, Inc. · 2022
- Descendant · cites it directly · 1 of its ownK211257 EFAI PACS Picture Archiving and Communication SystemEver Fortune.Ai, Co., Ltd. · 2021
- Descendant · 4 generations on · 0 of its ownK252539 Tempus PixelArterys, Inc. · 2025
Showing 5 of 6 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 6 · See all- K182034Arterys MICAArterys, Inc. · 2018 · cites it directly3descendants
- K192437Arterys MICAArterys, Inc. · 2020 · 2 generations on2descendants
- K203744Arterys MICAArterys, Inc. · 2022 · 3 generations on1descendant
- K211257EFAI PACS Picture Archiving and Communication SystemEver Fortune.Ai, Co., Ltd. · 2021 · cites it directly1descendant
- K252539Tempus PixelArterys, Inc. · 2025 · 4 generations on0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −4 | K922164 | Raytel Digital Imaging Systems | Olicon Imaging Systems, Inc. | 1993 | — |
| −3 | K973959 | Olicon Imaging Systems, Inc. 02-Workstation and/or Pacsview Software | Olicon Imaging Systems, Inc. | 1997 | — |
| −2 | K043146 | Horizon Medical Imaging | Mckesson Medical Imaging Company | 2005 | 11 |
| −1 | K152186 | HealthMyne PACS | Healthmyne, Inc. | 2015 | — |
| 0 (this device) | K171544 | Arterys Viewer | Arterys, Inc. | 2017 | — |
| +1 | K182034 | Arterys MICA | Arterys, Inc. | 2018 | — |
| +2 | K192437 | Arterys MICA | Arterys, Inc. | 2020 | — |
| +3 | K203744 | Arterys MICA | Arterys, Inc. | 2022 | — |
| +1 | K211257 | EFAI PACS Picture Archiving and Communication System | Ever Fortune.Ai, Co., Ltd. | 2021 | — |
| +4 | K252539 | Tempus Pixel | Arterys, Inc. | 2025 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1992 | 1 | 0 |
| 1993 | 1 | 0 |
| 1998 | 1 | 0 |
| 2002 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2018 | 1 | 0 |
| 2020 | 1 | 0 |
| 2021 | 1 | 0 |
| 2022 | 1 | 0 |
| 2023 | 1 | 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 LLZ? 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 LLZ device
- #1 K230955 syngo Application Softwarescore 21.5 · 11 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 |
|---|---|---|---|
| * | K152186 | HealthMyne PACSSummary page 4…Z Regulatory Class II 3. Predicate Device Primary Predicate Proprietary Name HealthMyne PACS Premarket Notification K152186 Classification Name System, Image Processing, Radiological Regulation Number 21 CFR 892.2050 Pr… | 2015 |
| † | K162513 | Arterys Software v2.0 | 2016 |
What descends from it? (6)
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 24 years and passes through 4 companies; a new generation was cleared every 7.0 years on median.
- 1 of the 8 ancestors has a recall of any class.
- Of its descendants, K182034 (Arterys, Inc., 2018) has gone furthest, with 3 descendants of its own.
How does its category compare?
All LLZ devicesLLZ System, Image Processing, Radiological: FDA decisions, review times, recalls and adverse event reports over 20 years. 2017, this device’s year, is highlighted.
FDA decisions per year · LLZ
58in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · LLZ
173in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · LLZ
11in 2025
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · LLZ
116in 2025
MAUDE reports naming product code LLZ, 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 | 76 | 36 | 20 | 152 |
| 2008 | 94 | 52 | 32 | 154 |
| 2009 | 70 | 62 | 21 | 145 |
| 2010 | 51 | 98 | 17 | 145 |
| 2011 | 106 | 79 | 30 | 454 |
| 2012 | 82 | 87 | 12 | 266 |
| 2013 | 95 | 84 | 64 | 1,130 |
| 2014 | 78 | 89 | 6 | 15,631 |
| 2015 | 64 | 90 | 16 | 211 |
| 2016 | 82 | 90 | 12 | 290 |
| 2017 | 78 | 107 | 5 | 104 |
| 2018 | 104 | 105 | 7 | 72 |
| 2019 | 74 | 107 | 2 | 88 |
| 2020 | 81 | 115 | 6 | 82 |
| 2021 | 83 | 116 | 3 | 70 |
| 2022 | 65 | 137 | 4 | 28 |
| 2023 | 87 | 157 | 8 | 26 |
| 2024 | 62 | 131 | 6 | 42 |
| 2025 | 58 | 173 | 11 | 116 |
| 2026 | 45 | 110 | 14 | — |
What is it indicated for?
Arterys Viewer is intended to be used as a Digital Imaging and Communications in Medicine (DICOM) and non-DICOM information and data management system. The Arterys Viewer displays, processes, stores, and transfers medical data from original equipment manufacturers (OEMs) that support the DICOM standard, with the exception of mammography. It provides the capability to store images and patient information from OEM equipment, and perform filtering, digital…
Read the full statement (134 words)
Arterys Viewer is intended to be used as a Digital Imaging and Communications in Medicine (DICOM) and non-DICOM information and data management system. The Arterys Viewer displays, processes, stores, and transfers medical data from original equipment manufacturers (OEMs) that support the DICOM standard, with the exception of mammography. It provides the capability to store images and patient information from OEM equipment, and perform filtering, digital manipulation and quantitative measurements.
The client software is designed to run on standard personal and business computers. The product is intended to be used by trained medical professionals, including but not limited to radiologists, oncologists, and physicians. It is intended to provide image and related information that is interpreted by a trained professional to render findings and/or diagnosis, but it does not directly generate any diagnosis or potential findings.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K171544 · printed Nov 6, 2026
Cite this page
510(k) Report. “K171544: Arterys Viewer.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K171544
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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