510(k) Report

510(k) · Cleared

Cleared

'All 2000' % Oxygen Analyzer

K002382510(k) TraditionalCleared Mar 14, 2001222-day reviewClass II21 CFR 868.1720

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

Analytical Industries, Inc. · CCL Analyzer, Gas, Oxygen, Gaseous-Phase

Cleared on Mar 14, 2001 after a 222-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 14, 2001
Review
222 days
Class
Class II
Product code
CCL
Recalls
None
Predicates
0

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

Descendants, by year cleared 2006: 1 descendant cleared200020052010201520202025
  1. This deviceK002382 'All 2000' % Oxygen AnalyzerAnalytical Industries, Inc. · 2001
  2. Descendant · cites it directly · 0 of its ownK053407 Oxygen Analyzer, Models Aii 20000A, Aii 2000HC, Aii 2000MAnalytical Industries, Inc. · 2006

Most influential descendants

Showing 1 of 1 · See all
  • K053407Oxygen Analyzer, Models Aii 20000A, Aii 2000HC, Aii 2000MAnalytical Industries, Inc. · 2006 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K002382'All 2000' % Oxygen AnalyzerAnalytical Industries, Inc.2001—
+1K053407Oxygen Analyzer, Models Aii 20000A, Aii 2000HC, Aii 2000MAnalytical Industries, Inc.2006—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200610
FIG. 1 — Lineage of K002382, 2001–2006Source: 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.

Planning a device in CCL? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new CCL device

  1. #1 K261389 PRO2 Elite Plus Oxygen Analyzer (PRO2PLUS-1)score 12.7 · 4 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin 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
K053407Oxygen Analyzer, Models Aii 20000A, Aii 2000HC, Aii 2000MAnalytical Industries, Inc.20060

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, K053407 (Analytical Industries, Inc., 2006) has gone furthest, with 0 descendants of its own.

How does its category compare?

All CCL devices

CCL Analyzer, Gas, Oxygen, Gaseous-Phase: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · CCL

2in 2025

2007: 22008: 22011: 12013: 22016: 12018: 12022: 22023: 12025: 22026 (partial year): 1
2007high 2 (2007) · low 0 (2009)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · CCL

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

Recalls per year · CCL

1in 2009

2009: 1
2007high 1 (2009) · low 0 (2007)2026

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

Adverse event reports per year · CCL

2in 2025

2007: 12008: 22009: 22010: 52011: 42012: 52013: 32014: 82015: 52016: 12017: 22018: 12019: 12020: 12021: 32023: 42024: 42025: 2
2007high 8 (2014) · low 0 (2022)2025

MAUDE reports naming product code CCL, 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—01
20082—02
20090—12
20100—05
20111—04
20120—05
20132—03
20140—08
20150—05
20161—01
20170—02
20181—01
20190—01
20200—01
20210—03
20222—00
20231—04
20240—04
20252—02
20261—0—
Cite this page

510(k) Report. “K002382: 'All 2000' % Oxygen Analyzer.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K002382

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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