510(k) · Cleared

Cleared

AX Workstation DR-Viewer Software Option

K992925510(k) TraditionalCleared Nov 23, 199985-day reviewClass II21 CFR 892.2050

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Siemens Corp. · LLZ System, Image Processing, Radiological

Cleared on Nov 23, 1999 as substantially equivalent to K990455 (Philips Medical Systems, Inc., 1999) and 1 other predicate after an 85-day review. Its family tree reaches back 1 generation to 1996.

Decided: Nov 23, 1999
Review: 85 days
Class: Class II
Product code: LLZ
Recalls: None
Predicates: 2

Its longest line of descent runs back 1 generation to K963980 (1996). 2 ancestors in all. No later device cites it as a predicate yet.

By dateBy generation

Root · 1 generation backK963980 Philips EasyvisionPhilips Medical Systems North America, Inc. · 1996 · Recalled
This deviceK992925 AX Workstation DR-Viewer Software OptionSiemens Corp. · 1999

View FIG. 1 as a table

Line of descent and top descendants

Generation	Number	Device	Applicant	Decided	Recalls
−1	K963980	Philips Easyvision	Philips Medical Systems North America, Inc.	1996	1
0 (this device)	K992925	AX Workstation DR-Viewer Software Option	Siemens Corp.	1999	—

Other ancestors by year cleared

Year cleared	Devices	With a Class I recall
1999	1	0

FIG. 1 — Lineage of K992925, 1996–1999Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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

Get a 510(k) 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	Applicant	Decided	Recalls
*	K990455	Philips Easy Vision Family Workstation Legs Option Summary page 2 …functions. The package is substantially equivalent to the following devices: Device Name FDA Clearance Number FDA Clearance Date Philips EasyVision Family Workstation K990455 5/12/99 Legs Option Philips Spine Option for EasyVision K963980 12/23/96 Workstation Information that substantiates this claim o…	Philips Medical Systems, Inc.	1999	—
*	K963980	Philips Easyvision Summary page 2 …owing devices: Device Name FDA Clearance Number FDA Clearance Date Philips EasyVision Family Workstation K990455 5/12/99 Legs Option Philips Spine Option for EasyVision K963980 12/23/96 Workstation Information that substantiates this claim of equivalence is provided throughout this 510(k) submission and…	Philips Medical Systems North America, Inc.	1996	1

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?

1 of the 2 ancestors has a recall of any class.

How does its category compare?

All LLZ devices

LLZ System, Image Processing, Radiological: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · LLZ

58in 2025

2007high 106 (2011) · low 51 (2010)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · LLZ

173in 2025

2007high 173 (2025) · low 36 (2007)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · LLZ

11in 2025

2007high 64 (2013) · low 2 (2019)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · LLZ

116in 2025

2007high 15,631 (2014) · low 26 (2023)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?

The AX Workstation DR-Viewer Software Option offers the user the ability to visualize composite images of selected anatomy (i.e. spine, legs, colon). The images produced by the package, as well as the measurement tools of DR-Viewer, are intended to assist the physician in diagnosis and treatment of musculoskeletal disorders and gastrointestinal conditions.

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/K992925 · printed Nov 6, 2026

Cite this page

510(k) Report. “K992925: AX Workstation DR-Viewer Software Option.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K992925

Report an extraction error

Are you the manufacturer?

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