510(k) Report

510(k) · Cleared

Cleared

Emit Ethyl Alcohol Assay

K903153510(k) TraditionalCleared Aug 9, 199022-day reviewClass II21 CFR 862.3040

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

Syva Co. · DIC Alcohol Dehydrogenase, Specific Reagent For Ethanol Enzyme Method

Cleared on Aug 9, 1990 after a 22-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 2 later devices descend from it.

Decided
Aug 9, 1990
Review
22 days
Class
Class II
Product code
DIC
Recalls
None
Predicates
0

2 later devices descend from it, 1 citing it directly.

Descendants, by year cleared 2000: 1 descendant cleared2001: 1 descendant cleared1990200020102020
  1. This deviceK903153 Emit Ethyl Alcohol AssaySyva Co. · 1990
  2. Descendant · cites it directly · 1 of its ownK993980 Syva Emit II Plus Ethyl Alcohol Assay, Models 9K309UL/9K409ULSyva Co. · 2000
  3. Descendant · 2 generations on · 0 of its ownK013538 EthanolAbbott Laboratories · 2001

Most influential descendants

Showing 2 of 2 · See all
  • K993980Syva Emit II Plus Ethyl Alcohol Assay, Models 9K309UL/9K409ULSyva Co. · 2000 · cites it directly1descendant
  • K013538EthanolAbbott Laboratories · 2001 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K903153Emit Ethyl Alcohol AssaySyva Co.1990—
+1K993980Syva Emit II Plus Ethyl Alcohol Assay, Models 9K309UL/9K409ULSyva Co.2000—
+2K013538EthanolAbbott Laboratories2001—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200010
200110
FIG. 1 — Lineage of K903153, 1990–2001Source: 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 DIC? 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 DIC device

  1. #1 K250609 Sober Self-Testscore 10.3 · 2 generations · no Class I recall
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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? (2)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K993980Syva Emit II Plus Ethyl Alcohol Assay, Models 9K309UL/9K409ULSyva Co.20001

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, K993980 (Syva Co., 2000) has gone furthest, with 1 descendant of its own.

How does its category compare?

All DIC devices

DIC Alcohol Dehydrogenase, Specific Reagent For Ethanol Enzyme Method: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · DIC

1in 2025

2007: 22010: 22011: 22012: 12013: 12018: 12025: 1
2007high 2 (2007) · low 0 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · DIC

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

Recalls per year · DIC

1in 2025

2010: 12025: 1
2007high 1 (2010) · low 0 (2007)2026

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

Adverse event reports per year · DIC

3in 2025

2009: 12010: 12011: 12020: 12025: 3
2007high 3 (2025) · low 0 (2007)2025

MAUDE reports naming product code DIC, 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
20080—00
20090—01
20102—11
20112—01
20121—00
20131—00
20140—00
20150—00
20160—00
20170—00
20181—00
20190—00
20200—01
20210—00
20220—00
20230—00
20240—00
20251—13
20260—0—
Cite this page

510(k) Report. “K903153: Emit Ethyl Alcohol Assay.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K903153

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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