510(k) · Cleared
ClearedSmartlight Digital Film Viewer, Models SL 4000PLUS, SL 2000PLUS
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Smartlight, Inc. · IXC Illuminator, Radiographic-Film
Cleared on Jun 1, 1999 as substantially equivalent to K952188 (Adp, Ltd., 1995) after a 46-day review. Its family tree reaches back 1 generation to 1995.
- Decided
- Jun 1, 1999
- Review
- 46 days
- Class
- Class I
- Product code
- IXC
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 1 generation to K952188 (1995). No later device cites it as a predicate yet.
- Root · 1 generation backK952188 Adviewer 2000Adp, Ltd. · 1995
- This deviceK991302 Smartlight Digital Film Viewer, Models SL 4000PLUS, SL 2000PLUSSmartlight, Inc. · 1999
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −1 | K952188 | Adviewer 2000 | Adp, Ltd. | 1995 | — |
| 0 (this device) | K991302 | Smartlight Digital Film Viewer, Models SL 4000PLUS, SL 2000PLUS | Smartlight, Inc. | 1999 | — |
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 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
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 |
|---|---|---|---|
| * | K952188 | Adviewer 2000Summary page 1…System Common or Usual Name: Radiographic Film Illuminator Classification Name: Radiographic Film Illuminator 3. Predicate Device Product: ADViewer Company: ADP Ltd. K952188 4. Device Description The Digital Film Viewer is a radiographic film illuminator designed to automatically adapt film-viewing c… | 1995 |
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?
- Its one ancestor has no recall.
- 1 other device also cites its predicate K952188.
How does its category compare?
All IXC devicesIXC 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 | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 0 | — | 0 | 0 |
| 2008 | 0 | — | 0 | 0 |
| 2009 | 0 | — | 0 | 0 |
| 2010 | 0 | — | 0 | 0 |
| 2011 | 0 | — | 0 | 0 |
| 2012 | 0 | — | 0 | 0 |
| 2013 | 0 | — | 0 | 0 |
| 2014 | 0 | — | 0 | 0 |
| 2015 | 0 | — | 0 | 0 |
| 2016 | 0 | — | 0 | 0 |
| 2017 | 0 | — | 0 | 0 |
| 2018 | 0 | — | 0 | 0 |
| 2019 | 0 | — | 0 | 0 |
| 2020 | 0 | — | 0 | 0 |
| 2021 | 0 | — | 0 | 0 |
| 2022 | 0 | — | 0 | 0 |
| 2023 | 0 | — | 0 | 0 |
| 2024 | 0 | — | 0 | 0 |
| 2025 | 0 | — | 0 | 0 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
The SmartLight Digital Film Viewer System is a radiographic film illuminator designed to automatically adapt film-viewing conditions to compensate for known physical and psychophysical limitations in human visual perception when reading radiographic films.
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/K991302 · printed Nov 5, 2026
Cite this page
510(k) Report. “K991302: Smartlight Digital Film Viewer, Models SL 4000PLUS, SL 2000PLUS.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K991302
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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