510(k) Report

510(k) · Cleared

Cleared

Chili Video, Chili Videopro

K000411510(k) AbbreviatedCleared Apr 14, 200066-day reviewClass II21 CFR 892.2030

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

Steinbeis-Transferzentrum Medizinische Informatik · LMA Digitizer, Image, Radiological

Cleared on Apr 14, 2000 after a 66-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 4 later devices descend from it.

Decided
Apr 14, 2000
Review
66 days
Class
Class II
Product code
LMA
Recalls
None
Predicates
0

4 later devices descend from it, 4 citing it directly.

Descendants, by year cleared 2013: 1 descendant cleared2001: 2 descendants cleared2004: 1 descendant cleared200020052010201520202025
  1. This deviceK000411 Chili Video, Chili VideoproSteinbeis-Transferzentrum Medizinische Informatik · 2000
  2. Descendant · cites it directly · 0 of its ownK132183 Dicom VideoBar Code Computer, Ltd. · 2013
  3. Descendant · cites it directly · 0 of its ownK033870 Image Management SystemWelch Allyn, Inc. · 2004
  4. Descendant · cites it directly · 0 of its ownK013631 Efilm VideoEfilm Medical, Inc. · 2001
  5. Descendant · cites it directly · 0 of its ownK013395 Lifejet Video LinkFerrania S.P.A. · 2001

Most influential descendants

Showing 4 of 4 · See all
  • K132183Dicom VideoBar Code Computer, Ltd. · 2013 · cites it directly0descendants
  • K033870Image Management SystemWelch Allyn, Inc. · 2004 · cites it directly0descendants
  • K013631Efilm VideoEfilm Medical, Inc. · 2001 · cites it directly0descendants
  • K013395Lifejet Video LinkFerrania S.P.A. · 2001 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K000411Chili Video, Chili VideoproSteinbeis-Transferzentrum Medizinische Informatik2000—
+1K132183Dicom VideoBar Code Computer, Ltd.2013—
+1K033870Image Management SystemWelch Allyn, Inc.2004—
+1K013631Efilm VideoEfilm Medical, Inc.2001—
+1K013395Lifejet Video LinkFerrania S.P.A.2001—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200120
200410
201310
FIG. 1 — Lineage of K000411, 2000–2013Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Get the monthly Device Review Tracker

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

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 LMA? 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
Get a 510(k) Report

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? (4)

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

NumberDeviceApplicantDecidedDescendants
K132183Dicom VideoBar Code Computer, Ltd.20130
K033870Image Management SystemWelch Allyn, Inc.20040
K013631Efilm VideoEfilm Medical, Inc.20010
K013395Lifejet Video LinkFerrania S.P.A.20010

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, K132183 (Bar Code Computer, Ltd., 2013) has gone furthest, with 0 descendants of its own.

How does its category compare?

All LMA devices

LMA Digitizer, Image, Radiological: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · LMA

3in 2013

2009: 12010: 22013: 3
2007high 3 (2013) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · LMA

80in 2013

2013: 80 days median
2007high 80 (2013)2026

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

Recalls per year · LMA

1in 2019

2019: 1
2007high 1 (2019) · low 0 (2007)2026

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

Adverse event reports per year · LMA

1in 2013

2008: 32012: 12013: 1
2007high 3 (2008) · low 0 (2007)2025

MAUDE reports naming product code LMA, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20070—00
20080—03
20091—00
20102—00
20110—00
20120—01
201338001
20140—00
20150—00
20160—00
20170—00
20180—00
20190—10
20200—00
20210—00
20220—00
20230—00
20240—00
20250—00
20260—0—

Recent decisions in LMA

The LMA category page

  • K132183Dicom VideoBar Code Computer, Ltd. · 2013
  • K130636Teleradpro Edge; Teleradpro Edge HD-CCDVidar Systems Corp. · 2013
  • K130406Diagnosticpro EdgeVidar Systems Corp. · 2013
  • K102476TeleradproVidar Systems Corp. · 2010
  • K093809Vidar Dental Film DigitizerVidar Systems Corp. · 2010

https://510kreport.com/device/K000411 · printed Nov 4, 2026

Cite this page

510(k) Report. “K000411: Chili Video, Chili Videopro.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K000411

Report an extraction error

Tell us what is wrong; we check it against the FDA summary.

Are you the manufacturer?

Send a correction or an update to this page, for example a newer model or a public statement about a recall.

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