510(k) Report

510(k) · Cleared

Cleared

Ecolyzer Carboximeter

K770209510(k) TraditionalCleared Mar 7, 197735-day reviewClass II21 CFR 864.7425

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

Iadec, Inc. · GHS Assay, Carboxyhemoglobin

Cleared on Mar 7, 1977 after a 35-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
Mar 7, 1977
Review
35 days
Class
Class II
Product code
GHS
Recalls
None
Predicates
0

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

Descendants, by year cleared 1998: 1 descendant cleared19801990200020102020
  1. This deviceK770209 Ecolyzer CarboximeterIadec, Inc. · 1977
  2. Descendant · cites it directly · 0 of its ownK974805 CO-Stat (TM) End Tidal Breath AnalyzerNatus Medical, Inc. · 1998

Most influential descendants

Showing 1 of 1 · See all
  • K974805CO-Stat (TM) End Tidal Breath AnalyzerNatus Medical, Inc. · 1998 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K770209Ecolyzer CarboximeterIadec, Inc.1977—
+1K974805CO-Stat (TM) End Tidal Breath AnalyzerNatus Medical, Inc.1998—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
199810
FIG. 1 — Lineage of K770209, 1977–1998Source: 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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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
K974805CO-Stat (TM) End Tidal Breath AnalyzerNatus Medical, Inc.19980

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, K974805 (Natus Medical, Inc., 1998) has gone furthest, with 0 descendants of its own.

How does its category compare?

All GHS devices

GHS Assay, Carboxyhemoglobin: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · GHS

FDA has decided no GHS device since 2007.

Median 510(k) review, days · GHS

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

Recalls per year · GHS

No recall names GHS since 2007.

Adverse event reports per year · GHS

No MAUDE report names GHS since 2007.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20070—00
20080—00
20090—00
20100—00
20110—00
20120—00
20130—00
20140—00
20150—00
20160—00
20170—00
20180—00
20190—00
20200—00
20210—00
20220—00
20230—00
20240—00
20250—00
20260—0—
Cite this page

510(k) Report. “K770209: Ecolyzer Carboximeter.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K770209

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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