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: PJD FDA class 2

Oral Fluid Drugs Of Abuse And Alcohol Test Specimen Collection Device

Clinical Chemistry

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The Oral Fluid Drugs of Abuse and Alcohol Test Specimen Collection Device is used for the collection, preservation, and transport of oral fluid specimens for drugs of abuse and alcohol testing in clinical and forensic settings. It is an FDA Class 2 device regulated under 21 CFR 862.1675, requiring 510(k) premarket notification, within the Clinical Chemistry (CH) medical specialty. The product code is PJD. This device is not an implant and is not life-sustaining.

510(k) Clearances

9 matches
K Number
Device Name
Quantisal™ Oral Fluid Collection Device
Quantisal™ II Oral Fluid Collection Device
Quantisal Oral Fluid Collection Device
Quantisal II Oral Fluid Collection Device
INTERCEPT ORAL FLUID DRUG TEST ORAL SPECIMEN COLLECTION DEVICE, MODEL 503-XXXX
ORAL-EZE ORAL FLUID COLLECTION SYSTEM
EPISCREEN ORAL SPECIMEN COLLECTION DEVICE
EPISCREEN
SALIVA SAMPLER

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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