510(k) Report

510(k) · Cleared

Recalled · Class II · 2014

Kodak Ektachem Clin. Chem. Slides (Trig)

K812029510(k) TraditionalCleared Aug 3, 198114-day reviewClass I21 CFR 862.1705Recalls 1

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

Eastman Kodak Company · CDT Lipase Hydrolysis/Glycerol Kinase Enzyme, Triglycerides

Cleared on Aug 3, 1981 after a 14-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 2 later devices descend from it. It has been recalled once.

Decided
Aug 3, 1981
Review
14 days
Class
Class I
Product code
CDT
Recalls
1
Predicates
0

2 later devices descend from it, 1 citing it directly.

Descendants, by year cleared 2013: 1 descendant cleared2019: 1 descendant cleared19801990200020102020
  1. This deviceK812029 Kodak Ektachem Clin. Chem. Slides (Trig)Eastman Kodak Company · 1981
  2. Descendant · cites it directly · 1 of its ownK130332 Vitros Chemistry Products Trig SlidesOrtho-Clinical Diagnostics, Inc. · 2013 · Recalled
  3. Descendant · 2 generations on · 0 of its ownK190490 VITROS XT Chemistry Products TRIG-CHOL SlidesOrtho-Clinical Diagnostics, Inc. · 2019

Most influential descendants

Showing 2 of 2 · See all
  • K130332Vitros Chemistry Products Trig SlidesOrtho-Clinical Diagnostics, Inc. · 2013 · cites it directly1descendant
  • K190490VITROS XT Chemistry Products TRIG-CHOL SlidesOrtho-Clinical Diagnostics, Inc. · 2019 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K812029Kodak Ektachem Clin. Chem. Slides (Trig)Eastman Kodak Company1981—
+1K130332Vitros Chemistry Products Trig SlidesOrtho-Clinical Diagnostics, Inc.20132
+2K190490VITROS XT Chemistry Products TRIG-CHOL SlidesOrtho-Clinical Diagnostics, Inc.2019—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201310
201910
FIG. 1 — Lineage of K812029, 1981–2019Source: 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), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

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  • 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)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K130332Vitros Chemistry Products Trig SlidesOrtho-Clinical Diagnostics, Inc.20131

Has anything in its family been recalled? (0 Class I)

Recalls of this device

DateClassRecallRoot causeReason
Nov 6, 2014Class IIZ-0848-2015Nonconforming Material/ComponentPotential for biased results using the specific lot of VITROS CHEMISTRY PRODUCTS TRIG slides.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • Of its descendants, K130332 (Ortho-Clinical Diagnostics, Inc., 2013) has gone furthest, with 1 descendant of its own.

How does its category compare?

All CDT devices

CDT Lipase Hydrolysis/Glycerol Kinase Enzyme, Triglycerides: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · CDT

1in 2015

2007: 12011: 12012: 12013: 22015: 1
2007high 2 (2013) · low 0 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · CDT

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

Recalls per year · CDT

1in 2021

2009: 12014: 22016: 32018: 12021: 1
2007high 3 (2016) · low 0 (2007)2026

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

Adverse event reports per year · CDT

12in 2025

2010: 32011: 112012: 42013: 12015: 62016: 122017: 32018: 42019: 22020: 22022: 42023: 72024: 52025: 12
2007high 12 (2016) · low 0 (2007)2025

MAUDE reports naming product code CDT, 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
20071—00
20080—00
20090—10
20100—03
20111—011
20121—04
20132—01
20140—20
20151—06
20160—312
20170—03
20180—14
20190—02
20200—02
20210—10
20220—04
20230—07
20240—05
20250—012
20260—0—
Cite this page

510(k) Report. “K812029: Kodak Ektachem Clin. Chem. Slides (Trig).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K812029

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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