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: CJW FDA class 2

Bromcresol Purple Dye-Binding, Albumin

Clinical Chemistry

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The Bromcresol Purple Dye-Binding, Albumin test system (product code CJW) is an in-vitro diagnostic device used in clinical chemistry to measure albumin concentrations in serum using the bromcresol purple (BCP) dye-binding colorimetric method. It is classified as FDA Class 2, indicating moderate risk, and requires a 510(k) premarket notification. It falls under regulation 21 CFR 862.1035 in the Clinical Chemistry medical specialty. This device is eligible for third-party review under the FDA's accredited persons program.

510(k) Clearances

18 matches
K Number
Device Name
Albumin BCP2
Albumin BCP
ADVIA CHEMISTRY ALBUMIN BCP REAGENT (ALBP), ADVIA CHEMISTRY ALBUMIN BCP CALIBRATOR
ALBUMIN REAGENT
RANDOX ALBUMIN
ALBUMIN BCG, MODEL AL 103-01
ALBP
ALBP
ABBOTT QUICKSTART ALBUMIN BCP (ALBP)#5A16
ALBUMIN REAGENT SET
ALBUMIN (BCP)
EMDS(TM) ALBUMIN TESTPACKS, #67652/95
VISION ALBUMIN
A-GENT LIQUID ALBUMIN
ALBUMIN BCP
WAKO AUTOMATED REAGENTS FOR HITACHI 705
ALBUMIN PROCEDURE BCP
QUANTIMETRIX BROMERESOL PURPLE ALBUMIN

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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