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: ECX FDA class 1

Cylinder, Compressed Gas, And Valve

Anesthesiology

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The Compressed Gas Cylinder and Valve is a container and control assembly used to store and dispense medical or dental gases such as oxygen, nitrous oxide, or nitrogen under pressure, used in anesthesia, sedation, and other clinical applications. It is classified as FDA Class 1, the lowest risk category, subject only to general controls and no premarket submission is required. The product code is ECX and the applicable regulation is 21 CFR 868.2700, under the Anesthesiology medical specialty.

510(k) Clearances

13 matches
K Number
Device Name
Intelli-Ox
Walk-O2-Bout
Medipure Oxygen-LC System
Intelli-Ox
OXYTOTE INFINITY SERIES VIPR SYSTEMS
GRAB 'N GO PLUS, GRAB 'N GO DIGITAL
EZ-OX PLUS GENERATION II
LIV LINDE INTERGRATED VALVE-PORTABLE OXYGEN SYSTEM, MODEL M706
LINDE INTEGRATED VALVE (LIV)
OX-SOX, MODEL C, D, E,
EZ-OX PLUS
MEDICYL-E-LITE PORTABLE OXYGEN DELIVERY SYSTEM
ALARM SYS FOR NITROUS OXIDE SYS.

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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