510(k) · Cleared

Cleared

Adviewer 2000

K952188510(k) TraditionalCleared May 30, 199521-day reviewClass I21 CFR 892.1890

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

Adp, Ltd. · IXC Illuminator, Radiographic-Film

Cleared on May 30, 1995 after a 21-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 2 later devices descend from it.

Decided: May 30, 1995
Review: 21 days
Class: Class I
Product code: IXC
Recalls: None
Predicates: 0

2 later devices descend from it, 2 citing it directly.

This deviceK952188 Adviewer 2000Adp, Ltd. · 1995
Descendant · cites it directly · 0 of its ownK991302 Smartlight Digital Film Viewer, Models SL 4000PLUS, SL 2000PLUSSmartlight, Inc. · 1999
Descendant · cites it directly · 0 of its ownK973965 Smart Motorized ViewerSmartlight, Ltd. · 1997

Most influential descendants

Showing 2 of 2 · See all

K991302Smartlight Digital Film Viewer, Models SL 4000PLUS, SL 2000PLUSSmartlight, Inc. · 1999 · cites it directly0descendants
K973965Smart Motorized ViewerSmartlight, Ltd. · 1997 · cites it directly0descendants

View FIG. 1 as a table

Line of descent and top descendants

Generation	Number	Device	Applicant	Decided	Recalls
0 (this device)	K952188	Adviewer 2000	Adp, Ltd.	1995	—
+1	K991302	Smartlight Digital Film Viewer, Models SL 4000PLUS, SL 2000PLUS	Smartlight, Inc.	1999	—
+1	K973965	Smart Motorized Viewer	Smartlight, Ltd.	1997	—

Descendants by year cleared

Year cleared	Devices	With a Class I recall
1997	1	0
1999	1	0

FIG. 1 — Lineage of K952188, 1995–1999Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Sources: FDA 510(k) database (decision fields), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in IXC? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Candidate predicates for a device like this, rankedin the report
Recall history across each candidate’s familyin the report

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What was it cleared against?

FDA has not posted a summary or statement for it, so its predicates are not known.

What descends from it? (2)

2 later devices cite it directly; ranked here by how many devices descend from each in turn.

Number	Device	Applicant	Decided	Descendants
K991302	Smartlight Digital Film Viewer, Models SL 4000PLUS, SL 2000PLUS	Smartlight, Inc.	1999	0
K973965	Smart Motorized Viewer	Smartlight, Ltd.	1997	0

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?

Of its descendants, K991302 (Smartlight, Inc., 1999) has gone furthest, with 0 descendants of its own.

How does its category compare?

All IXC devices

IXC Illuminator, Radiographic-Film: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · IXC

FDA has decided no IXC device since 2007.

Median 510(k) review, days · IXC

Too few IXC 510(k)s in any year since 2007 to give a median.

Recalls per year · IXC

No recall names IXC since 2007.

Adverse event reports per year · IXC

No MAUDE report names IXC since 2007.

View these four charts as a table

Year	Median 510(k) review, days	MAUDE reports
2007	—	0
2008	—	0
2009	—	0
2010	—	0
2011	—	0
2012	—	0
2013	—	0
2014	—	0
2015	—	0
2016	—	0
2017	—	0
2018	—	0
2019	—	0
2020	—	0
2021	—	0
2022	—	0
2023	—	0
2024	—	0
2025	—	0
2026	—	—

https://510kreport.com/device/K952188 · printed Nov 5, 2026

Cite this page

510(k) Report. “K952188: Adviewer 2000.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K952188

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Record history

FDA decision record loaded May 2, 2026
Lineage and recalls computed Nov 3, 2026
Page last updated Nov 3, 2026