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.

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Describe your device and the Research Assistant searches 510(k)s, compares intended use, and drafts a predicate shortlist — with citations.

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Product Code: CIE FDA class 2

Volumetric/Manometric, Carbon-Dioxide

Clinical Chemistry

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The Volumetric/Manometric, Carbon Dioxide test system (product code CIE) is an in-vitro diagnostic device used in clinical chemistry to measure total carbon dioxide or bicarbonate in biological specimens using volumetric or manometric physical measurement techniques, supporting acid-base evaluation. It is classified as FDA Class 2, indicating moderate risk, and requires a 510(k) premarket notification. It falls under regulation 21 CFR 862.1160 in the Clinical Chemistry medical specialty. This device is eligible for third-party review under the FDA's accredited persons program.

510(k) Clearances

7 matches
K Number
Device Name
P/N 35310, IL TEST ALKALINE PHOSPHATASE REAGENT
MICRO CO2 APPARATUS
CO2 REAGENT SET
TOTAL CO2 REAGENT SET
AIRMED SMOKE EVACUATION & FILTER
SERALYZER REFLECTANCE PHOTOMETER/CALIB.
CARBON DIOXIDE ANALYZER

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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