510(k) Report

510(k) · Cleared

Cleared

Breathscan, Breath and Breath Check Alcohol Detectors

K060761510(k) TraditionalCleared Apr 28, 200638-day reviewClass I21 CFR 862.3050

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

Akers Biosciences, Inc. · DJZ Devices, Breath Trapping, Alcohol

Cleared on Apr 28, 2006 as substantially equivalent to K052448 (Connectables, LLC, 2006) after a 38-day review. Its family tree reaches back 3 generations to 2004. 3 later devices descend from it.

Decided
Apr 28, 2006
Review
38 days
Class
Class I
Product code
DJZ
Recalls
None
Predicates
1

Its longest line of descent runs back 3 generations to K041334 (2004). 3 later devices descend from it, 3 citing it directly.

Descendants, by year cleared 2009: 1 descendant cleared2011: 1 descendant cleared2010: 1 descendant clearedK041334 · Alcomate, Model CA2000 · Khn Solutions, LLC · 2004K043188 · Alcohawk Precision · Q3 Innovations, LLC · 2005K052448 · Pocket Breathalyzer. Connectables · Connectables, LLC · 2006200020052010201520202025
  1. Root · 3 generations backK041334 Alcomate, Model CA2000Khn Solutions, LLC · 2004
  2. 2 generations backK043188 Alcohawk PrecisionQ3 Innovations, LLC · 2005
  3. 1 generation backK052448 Pocket Breathalyzer. ConnectablesConnectables, LLC · 2006
  4. This deviceK060761 Breathscan, Breath and Breath Check Alcohol DetectorsAkers Biosciences, Inc. · 2006
  5. Descendant · cites it directly · 0 of its ownK102225 Alco-Breath Tube, Checkpoint Breath Alcohol TestAlcopro, Inc. · 2011
  6. Descendant · cites it directly · 0 of its ownK093143 Mission Breath Alcohol DetectorACON Laboratories, Inc. · 2010 · Recalled
  7. Descendant · cites it directly · 0 of its ownK082080 Alco Tube PlusAlcotest Quebec · 2009

Most influential descendants

Showing 3 of 3 · See all
  • K102225Alco-Breath Tube, Checkpoint Breath Alcohol TestAlcopro, Inc. · 2011 · cites it directly0descendants
  • K093143Mission Breath Alcohol DetectorACON Laboratories, Inc. · 2010 · cites it directly0descendants
  • K082080Alco Tube PlusAlcotest Quebec · 2009 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−3K041334Alcomate, Model CA2000Khn Solutions, LLC2004—
−2K043188Alcohawk PrecisionQ3 Innovations, LLC2005—
−1K052448Pocket Breathalyzer. ConnectablesConnectables, LLC2006—
0 (this device)K060761Breathscan, Breath and Breath Check Alcohol DetectorsAkers Biosciences, Inc.2006—
+1K102225Alco-Breath Tube, Checkpoint Breath Alcohol TestAlcopro, Inc.2011—
+1K093143Mission Breath Alcohol DetectorACON Laboratories, Inc.20101
+1K082080Alco Tube PlusAlcotest Quebec2009—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200910
201010
201110
FIG. 1 — Lineage of K060761, 2004–2011Source: 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), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in DJZ? 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
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What was it cleared against? (1)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.

TypeNumberDeviceApplicantDecidedRecalls
*K052448Pocket Breathalyzer. Connectables
Summary page 1
…lation Number: 862.3050 5.4 Predicate Device: BreathScan is equivalent to: CONNECTABLES® Alcohol Tester manufactured by Connectables, LLC in Waukegan, IL (K052448). 5.5 Indications for Use The BreathScan® Alcohol Detector is an in vitro medical device to qualitatively detect…
Connectables, LLC2006—

Also cleared against K052448: 3 other devices →

What descends from it? (3)

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

NumberDeviceApplicantDecidedDescendants
K102225Alco-Breath Tube, Checkpoint Breath Alcohol TestAlcopro, Inc.20110
K093143Mission Breath Alcohol DetectorACON Laboratories, Inc.20100
K082080Alco Tube PlusAlcotest Quebec20090

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?

  • The line of descent spans 2 years and passes through 4 companies; a new generation was cleared every 6 months on median.
  • None of the 3 ancestors has a recall.
  • Of its descendants, K102225 (Alcopro, Inc., 2011) has gone furthest, with 0 descendants of its own.
  • 3 other devices also cite its predicate K052448.

How does its category compare?

All DJZ devices

DJZ Devices, Breath Trapping, Alcohol: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · DJZ

1in 2016

2007: 22008: 52009: 52010: 22011: 32013: 12016: 1
2007high 5 (2008) · low 0 (2012)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · DJZ

240in 2011

2008: 149 days median2009: 122 days median2011: 240 days median
2007high 240 (2011) · low 122 (2009)2026

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

Recalls per year · DJZ

1in 2007

2007: 1
2007high 1 (2007) · low 0 (2008)2026

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

Adverse event reports per year · DJZ

3in 2025

2007: 22011: 12019: 12022: 12023: 12025: 3
2007high 3 (2025) · low 0 (2008)2025

MAUDE reports naming product code DJZ, 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—12
2008514900
2009512200
20102—00
2011324001
20120—00
20131—00
20140—00
20150—00
20161—00
20170—00
20180—00
20190—01
20200—00
20210—00
20220—01
20230—01
20240—00
20250—03
20260—0—

What is it indicated for?

The BreathScan® Alcohol Detector is an in vitro medical device to qualitatively detect the presence of alcohol in the human breath. It is a disposable screening device for one-time use. The detector is available at several detection cut-offs including 0.02, 0.04, 0.05, and 0.08 percent breath alcohol. The device is used only as a screening device and is only an indication of the possible presence of alcohol in the blood of the test subject.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K060761: Breathscan, Breath and Breath Check Alcohol Detectors.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K060761

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Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026