510(k) · Cleared
ClearedAlz Web Pacs, Version 1.0
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Alz, Inc. · LLZ System, Image Processing, Radiological
Cleared on Jun 11, 2008 as substantially equivalent to K020995 (Efilm Medical, Inc., 2002) and 1 other predicate after a 34-day review. Its family tree reaches back 5 generations to 1990. 8 later devices descend from it.
- Decided
- Jun 11, 2008
- Review
- 34 days
- Class
- Class II
- Product code
- LLZ
- Recalls
- None
- Predicates
- 2
Its longest line of descent runs back 5 generations to K896095 (1990). 7 ancestors in all. 8 later devices descend from it, 1 citing it directly.
- Root · 5 generations backK896095 Images-on-Call Teleradiology SystemDevices & Services Co. · 1990
- 4 generations backK962699 Radworks Medical Imaging SoftwareApplicare Medical Imaging, B.V. · 1996
- 3 generations backK982862 Radworks Medical Imaging Software with Quality Control ModuleApplicare Medical Imaging, B.V. · 1998
- 2 generations backK012211 Efilm WorkstationEfilm Medical, Inc. · 2001 · Recalled
- 1 generation backK020995 Efilm Workstation with ModulesEfilm Medical, Inc. · 2002 · Recalled
- This deviceK081304 Alz Web Pacs, Version 1.0Alz, Inc. · 2008
- Descendant · cites it directly · 7 of its ownK130624 CONIGlobalmed · 2013
- Descendant · 2 generations on · 4 of its ownK153653 DICOM ViewerBrainlab AG · 2016
- Descendant · 3 generations on · 3 of its ownK191014 Elements ViewerBrainlab AG · 2020
- Descendant · 4 generations on · 1 of its ownK232759 Viewer (5.4); Elements Viewer; Mixed Reality Viewer; Smart Layout…Brainlab AG · 2024 · Recalled
- Descendant · 2 generations on · 1 of its ownK132763 Advanced ViewerBrainlab AG · 2014
Showing 5 of 8 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 8 · See all- K130624CONIGlobalmed · 2013 · cites it directly7descendants
- K153653DICOM ViewerBrainlab AG · 2016 · 2 generations on4descendants
- K191014Elements ViewerBrainlab AG · 2020 · 3 generations on3descendants
- K232759Viewer (5.4); Elements Viewer; Mixed Reality Viewer; Smart Layout; Elements Viewer Smart…Brainlab AG · 2024 · 4 generations on1descendant
- K132763Advanced ViewerBrainlab AG · 2014 · 2 generations on1descendant
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −5 | K896095 | Images-on-Call Teleradiology System | Devices & Services Co. | 1990 | — |
| −4 | K962699 | Radworks Medical Imaging Software | Applicare Medical Imaging, B.V. | 1996 | — |
| −3 | K982862 | Radworks Medical Imaging Software with Quality Control Module | Applicare Medical Imaging, B.V. | 1998 | — |
| −2 | K012211 | Efilm Workstation | Efilm Medical, Inc. | 2001 | 1 |
| −1 | K020995 | Efilm Workstation with Modules | Efilm Medical, Inc. | 2002 | 2 |
| 0 (this device) | K081304 | Alz Web Pacs, Version 1.0 | Alz, Inc. | 2008 | — |
| +1 | K130624 | CONI | Globalmed | 2013 | — |
| +2 | K153653 | DICOM Viewer | Brainlab AG | 2016 | — |
| +3 | K191014 | Elements Viewer | Brainlab AG | 2020 | — |
| +4 | K232759 | Viewer (5.4); Elements Viewer; Mixed Reality Viewer; Smart Layout; Elements… | Brainlab AG | 2024 | 1 |
| +2 | K132763 | Advanced Viewer | Brainlab AG | 2014 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1991 | 1 | 0 |
| 2003 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2013 | 1 | 0 |
| 2014 | 2 | 0 |
| 2016 | 1 | 0 |
| 2020 | 1 | 0 |
| 2024 | 1 | 0 |
| 2025 | 1 | 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 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? (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 |
|---|---|---|---|
| * | K020995 | Efilm Workstation with ModulesSummary page 1…ommunication system Product Code LLZ 21 CFR Regulation 892.2050 3. PREDICATE DEVICE · eFILM Workstation with Modules, K020995, Merge eMED, Inc. · UniPACS, K023476, Universal PACS, Inc. 4. DEVICE DESCRIPTION The ALZ Web PACS (Version 1.0)… | 2002 |
| * | K023476 | Unipacs WorkstationSummary page 1…LLZ 21 CFR Regulation 892.2050 3. PREDICATE DEVICE · eFILM Workstation with Modules, K020995, Merge eMED, Inc. · UniPACS, K023476, Universal PACS, Inc. 4. DEVICE DESCRIPTION The ALZ Web PACS (Version 1.0) is designed for the management, viewing, and… | 2003 |
What descends from it? (8)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K130624 | CONI | 2013 | 7 |
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 18 years and passes through 4 companies; a new generation was cleared every 2.8 years on median.
- 2 of the 7 ancestors have a recall of any class.
- Of its descendants, K130624 (Globalmed, 2013) has gone furthest, with 7 descendants of its own.
- 14 other devices also cite its predicate K020995.
How does its category compare?
All LLZ devicesLLZ System, Image Processing, Radiological: FDA decisions, review times, recalls and adverse event reports over 20 years. 2008, 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?
ALZ Web PACS (Version 1.0) is an imaging software system intended to be used by trained healthcare professionals. ALZ Web PACS is used with general purpose computing hardware to acquire, transmit, store, view, and process DICOM images.
This device is not intended for mammography.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K081304 · printed Nov 4, 2026
Cite this page
510(k) Report. “K081304: Alz Web Pacs, Version 1.0.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K081304
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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