510(k) Report

510(k) · Cleared

Cleared

Vitalograph - Breathco Monitor

K902113510(k) TraditionalCleared Oct 26, 1990168-day reviewClass II21 CFR 868.1430

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

Mcneill Intl., Inc. · CCJ Analyzer, Gas, Carbon-Monoxide, Gaseous-Phase

Cleared on Oct 26, 1990 after a 168-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
Oct 26, 1990
Review
168 days
Class
Class II
Product code
CCJ
Recalls
None
Predicates
0

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

Descendants, by year cleared 1998: 1 descendant cleared1990200020102020
  1. This deviceK902113 Vitalograph - Breathco MonitorMcneill Intl., Inc. · 1990
  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)K902113Vitalograph - Breathco MonitorMcneill Intl., Inc.1990—
+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 K902113, 1990–1998Source: 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.

Planning a device in CCJ? 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 CCJ device

  1. #1 K253119 CoSense ETCO Monitorscore 12.6 · 5 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin 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? (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 CCJ devices

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

FDA decisions per year · CCJ

2in 2021

2008: 22010: 12012: 12014: 12015: 12017: 12018: 12019: 12021: 22026 (partial year): 1
2007high 2 (2008) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · CCJ

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

Recalls per year · CCJ

No recall names CCJ since 2007.

Adverse event reports per year · CCJ

No MAUDE report names CCJ since 2007.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20070—00
20082—00
20090—00
20101—00
20110—00
20121—00
20130—00
20141—00
20151—00
20160—00
20171—00
20181—00
20191—00
20200—00
20212—00
20220—00
20230—00
20240—00
20250—00
20261—0—
Cite this page

510(k) Report. “K902113: Vitalograph - Breathco Monitor.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K902113

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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