510(k) Report

510(k) · Cleared

Recalled · Class II · 2013

Vitro Chemistry Products ECO2 Slide & Calibrator Kit 2

K001133510(k) SpecialCleared Apr 24, 200014-day reviewClass II21 CFR 862.1160Recalls 1

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

Ortho-Clinical Diagnostics, Inc. · KHS Enzymatic, Carbon-Dioxide

Cleared on Apr 24, 2000 after a 14-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 4 later devices descend from it. It has been recalled once.

Decided
Apr 24, 2000
Review
14 days
Class
Class II
Product code
KHS
Recalls
1
Predicates
0

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

Descendants, by year cleared 2010: 1 descendant cleared2012: 1 descendant cleared2018: 1 descendant cleared2019: 1 descendant cleared200020052010201520202025
  1. This deviceK001133 Vitro Chemistry Products ECO2 Slide & Calibrator Kit 2Ortho-Clinical Diagnostics, Inc. · 2000
  2. Descendant · cites it directly · 2 of its ownK120765 Vitros Chemistry Products ECO2 SlidesOrtho-Clinical Diagnostics, Inc. · 2012 · Recalled
  3. Descendant · 2 generations on · 1 of its ownK182072 VITROS Chemistry Products Cl-Slides, VITROS Chemistry Products ECO2…Ortho-Clinical Diagnostics, Inc. · 2018 · Recalled
  4. Descendant · 3 generations on · 0 of its ownK190520 VITROS XT Chemistry Products GLU-Ca SlidesOrtho-Clinical Diagnostics, Inc. · 2019
  5. Descendant · cites it directly · 0 of its ownK093611 Vitros Chemistry Products CO2 DT Slides; Vitros Chemmistry Products…Ortho-Clinical Diagnostics, Inc. · 2010

Most influential descendants

Showing 4 of 4 · See all
  • K120765Vitros Chemistry Products ECO2 SlidesOrtho-Clinical Diagnostics, Inc. · 2012 · cites it directly2descendants
  • K182072VITROS Chemistry Products Cl-Slides, VITROS Chemistry Products ECO2 Slides, VITROS…Ortho-Clinical Diagnostics, Inc. · 2018 · 2 generations on1descendant
  • K190520VITROS XT Chemistry Products GLU-Ca SlidesOrtho-Clinical Diagnostics, Inc. · 2019 · 3 generations on0descendants
  • K093611Vitros Chemistry Products CO2 DT Slides; Vitros Chemmistry Products DT Calibrator Kit…Ortho-Clinical Diagnostics, Inc. · 2010 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K001133Vitro Chemistry Products ECO2 Slide & Calibrator Kit 2Ortho-Clinical Diagnostics, Inc.2000—
+1K120765Vitros Chemistry Products ECO2 SlidesOrtho-Clinical Diagnostics, Inc.20121
+2K182072VITROS Chemistry Products Cl-Slides, VITROS Chemistry Products ECO2 Slides…Ortho-Clinical Diagnostics, Inc.20182
+3K190520VITROS XT Chemistry Products GLU-Ca SlidesOrtho-Clinical Diagnostics, Inc.2019—
+1K093611Vitros Chemistry Products CO2 DT Slides; Vitros Chemmistry Products DT…Ortho-Clinical Diagnostics, Inc.2010—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201010
201210
201810
201910
FIG. 1 — Lineage of K001133, 2000–2019Source: 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? (4)

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

NumberDeviceApplicantDecidedDescendants
K120765Vitros Chemistry Products ECO2 SlidesOrtho-Clinical Diagnostics, Inc.20122
K093611Vitros Chemistry Products CO2 DT Slides; Vitros Chemmistry Products DT Calibrator Kit…Ortho-Clinical Diagnostics, Inc.20100

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

Recalls of this device

DateClassRecallRoot causeReason
Jun 12, 2013Class IIZ-0312-2014Equipment maintenanceOrtho Clinical Diagnostics is recalling Slide Dispense cartridges used with some VITROS Chemistry Product Slides due to slide dispense issues.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • Of its descendants, K120765 (Ortho-Clinical Diagnostics, Inc., 2012) has gone furthest, with 2 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. “K001133: Vitro Chemistry Products ECO2 Slide & Calibrator Kit 2.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K001133

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