Tool · 510(k)

510(k) Predicate Finder

Find potential predicate devices for your 510(k) submission. Enter a K-number to find all clearances with the same product code, a three-letter product code to browse clearances directly, or search by device name.

Product Code: DJZ FDA class 1

Devices, Breath Trapping, Alcohol

Clinical Toxicology

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Breath Trapping Devices for Alcohol are collection devices designed to capture and preserve exhaled breath samples for subsequent laboratory analysis of ethanol content, supporting forensic and clinical toxicology investigations of alcohol exposure. This device is classified as FDA Class 1, indicating low risk, and is subject only to general controls without premarket notification requirements. It is regulated under 21 CFR 862.3050 within the Clinical Toxicology specialty.

510(k) Clearances

28 matches
K Number
Device Name
Soberlink Cellular Device and Sober Sky Web Portal
PAS ALCOVISOR MARS, PAS ALCOVISOR SATELLITE
PAD (PERSONAL ALCOHOL DETECTOR) BREATH ALCOHOL TEST SYSTEM
ALCO-BREATH TUBE, CHECKPOINT BREATH ALCOHOL TEST
BREATHSCN PRO
CONTRALCO
MISSION BREATH ALCOHOL DETECTOR
ALCODIGITAL BREATHALYZER, MODEL AT576, AT577, AT578, AT579
LIFEGUARD BACKTRACK B90 BREATH ALCOHOL TESTER
ALCO TUBE PLUS
BACTRACK SELECT BREATHALYZER, MODEL S80
BACTRACK SELECT BREATHALYZER, MODELS S30, S50, S70
KEY RING ALCOHOL BREATHALYZER
IMPAIR AWARE ALCOHOL LEVEL INDICATION SYSTEM (ALIS)
ALCOHAWK MODEL PT500 DIGITAL ALCOHOL DETECTOR
DRAEGER ALCOTEST 6510
REDLINE ALCOHOL BREATH TESTER
BACTRACK LCD ALCOHOL DETECTOR
RMI LCD ALCOHOL DETECTOR
BREATH ALCOHOL CHECK .02 AND BREATHSCAN .02 DETECTION SYSTEMS
BREATH ALCOHOL TEST SYSTEM, MODEL AL-5000
BREATH ALCOHOL TEST SYSTEM, MODEL AL-6000
BREATHSCAN, BREATH AND BREATH CHECK ALCOHOL DETECTORS
POCKET BREATHALYZER. CONNECTABLES
BREATH ALCOHOL TEST SYSTEM, MODEL AL 2500
BREATHKEY MODEL G10/BREATHKEY MODEL G30X
ALCOHAWK PRECISION
ALCOMATE, MODEL CA2000

What is a Predicate Device?

A predicate device is a legally marketed device that a new 510(k) applicant uses to demonstrate substantial equivalence. The FDA's 510(k) pathway requires manufacturers to show that their device has the same intended use and similar technological characteristics as one or more predicate devices already cleared for commercial distribution.

Finding the right predicate is a critical step in 510(k) strategy. Manufacturers typically search for cleared devices with the same FDA product code, which groups devices by their intended use and regulatory classification. This tool helps you identify potential predicates by browsing all clearances within a product code.

Note that predicate devices must be legally marketed — they cannot be devices that were cleared but never commercialized, or devices subject to a mandatory recall. The determination of substantial equivalence considers intended use, technological characteristics, and performance data.

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