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: LFP FDA class 2

Conductivity Rate, Urea Nitrogen

Clinical Chemistry

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A conductivity rate test for urea nitrogen is a clinical chemistry laboratory device that measures blood urea nitrogen (BUN) levels using conductivity-based principles, providing an indicator of renal function and nitrogen metabolism. The device is FDA Class 2, indicating moderate risk and requiring 510(k) premarket notification. It carries product code LFP and is regulated under 21 CFR 862.1770 within the Clinical Chemistry specialty. This device is eligible for third-party review.

510(k) Clearances

6 matches
K Number
Device Name
GAMBRO DQM 200
HICHEM BUN REAGENT
SIGMA DIAGNOSTICS BUN REAGENT
SIGMA BUN REAGENT
BUN REAGENT KIT
LIQUILYME BUN REAGENT

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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