510(k) Report

510(k) · Cleared

Cleared

Demetra Analytics Toolkit

K201408510(k) TraditionalCleared Feb 18, 2021266-day reviewClass II21 CFR 878.4580

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

Barco N.V. · PSN Light Based Imaging

Cleared on Feb 18, 2021 as substantially equivalent to K062736 (Astron Clinica Limited, 2007) after a 266-day review. Its family tree reaches back 2 generations to 2003.

Decided
Feb 18, 2021
Review
266 days
Class
Class II
Product code
PSN
Recalls
None
Predicates
1

Its longest line of descent runs back 2 generations to K023729 (2003). No later device cites it as a predicate yet.

  1. Root · 2 generations backK023729 Siascope IIAstron Clinica Limited · 2003
  2. 1 generation backK062736 Siascope VAstron Clinica Limited · 2007
  3. This deviceK201408 Demetra Analytics ToolkitBarco N.V. · 2021
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−2K023729Siascope IIAstron Clinica Limited2003—
−1K062736Siascope VAstron Clinica Limited2007—
0 (this device)K201408Demetra Analytics ToolkitBarco N.V.2021—
FIG. 1 — Lineage of K201408, 2003–2021Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

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 PSN? 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 PSN device

  1. #1 K230448 DeepX DermoSight Dermatoscopescore 6.2 · 4 generations · no Class I recall
  2. #2 Held for the reportin the report
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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.

TypeNumberDeviceApplicantDecidedRecalls
*K062736Siascope V
Summary page 4
…Regulation number: 878.4580 Regulatory class: 2 5. Predicate SIAscope V - Astron Clinica Limited - K062736 device 6. Device The Barco Demetra Analytics Toolkit is a software application used to support analysis of des…
Astron Clinica Limited2007—

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?

  • The line of descent spans 18 years and passes through 2 companies; a new generation was cleared every 13.4 years on median.
  • None of the 2 ancestors has a recall.

How does its category compare?

All PSN devices

PSN Light Based Imaging: FDA decisions, review times, recalls and adverse event reports over 20 years. 2021, this device’s year, is highlighted.

FDA decisions per year · PSN

1in 2023

2007: 12008: 12018: 12019: 12021: 12022: 12023: 1
2007high 1 (2007) · low 0 (2009)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · PSN

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

Recalls per year · PSN

No recall names PSN since 2007.

Adverse event reports per year · PSN

No MAUDE report names PSN since 2007.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20071—00
20081—00
20090—00
20100—00
20110—00
20120—00
20130—00
20140—00
20150—00
20160—00
20170—00
20181—00
20191—00
20200—00
20211—00
20221—00
20231—00
20240—00
20250—00
20260—0—

What is it indicated for?

The Barco Demetra Analytics Toolkit is a non-invasive skin analysis system. The Barco Demetra Skin Parameter Maps Tool provides maps that show the relative location of blood and pigment. The Barco Demetra Skin Parameter Maps Tool is intended only to complement dermoscopy.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K201408: Demetra Analytics Toolkit.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K201408

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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