510(k) Report

510(k) · Cleared

Cleared

Kodak Ektachem Clinical Chemistry Slides (ECO2)

K903144510(k) TraditionalCleared Sep 25, 199069-day reviewClass II21 CFR 862.1160

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

Eastman Kodak Company · KHS Enzymatic, Carbon-Dioxide

Cleared on Sep 25, 1990 after a 69-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 1 later device descends from it.

Decided
Sep 25, 1990
Review
69 days
Class
Class II
Product code
KHS
Recalls
None
Predicates
0

1 later device descends from it, 1 citing it directly.

Descendants, by year cleared 1999: 1 descendant cleared1990200020102020
  1. This deviceK903144 Kodak Ektachem Clinical Chemistry Slides (ECO2)Eastman Kodak Company · 1990
  2. Descendant · cites it directly · 0 of its ownK992475 Careside CO2, TotalCareside, Inc. · 1999

Most influential descendants

Showing 1 of 1 · See all
  • K992475Careside CO2, TotalCareside, Inc. · 1999 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K903144Kodak Ektachem Clinical Chemistry Slides (ECO2)Eastman Kodak Company1990—
+1K992475Careside CO2, TotalCareside, Inc.1999—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
199910
FIG. 1 — Lineage of K903144, 1990–1999Source: 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 KHS? 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? (1)

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

NumberDeviceApplicantDecidedDescendants
K992475Careside CO2, TotalCareside, Inc.19990

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, K992475 (Careside, Inc., 1999) has gone furthest, with 0 descendants of its own.

How does its category compare?

All KHS devices

KHS Enzymatic, Carbon-Dioxide: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · KHS

1in 2017

2007: 22008: 12009: 12010: 32011: 12012: 22013: 22014: 12016: 12017: 1
2007high 3 (2010) · low 0 (2015)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · KHS

143in 2010

2010: 143 days median
2007high 143 (2010)2026

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

Recalls per year · KHS

1in 2025

2013: 12019: 12023: 12025: 1
2007high 1 (2013) · low 0 (2007)2026

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

Adverse event reports per year · KHS

40in 2025

2008: 22009: 142011: 52012: 32013: 22014: 62015: 12016: 42017: 72018: 152019: 352020: 312021: 142022: 102023: 252024: 302025: 40
2007high 40 (2025) · low 0 (2007)2025

MAUDE reports naming product code KHS, 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
20072—00
20081—02
20091—014
2010314300
20111—05
20122—03
20132—12
20141—06
20150—01
20161—04
20171—07
20180—015
20190—135
20200—031
20210—014
20220—010
20230—125
20240—030
20250—140
20260—0—
Cite this page

510(k) Report. “K903144: Kodak Ektachem Clinical Chemistry Slides (ECO2).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K903144

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