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: CAX FDA class 1

Flowmeter, Tube, Thorpe, Back-Pressure Compensated

Anesthesiology

View full classification →

The Back-Pressure Compensated Thorpe Tube Flowmeter is an anesthesiology device used to measure and control the flow rate of medical gases such as oxygen or nitrous oxide delivered to patients, with compensation mechanisms that maintain accuracy regardless of downstream pressure changes. It is classified as FDA Class 1 (lowest risk), subject only to general controls, and is exempt from premarket notification. The product code is CAX, regulated under 21 CFR 868.2340, within the Anesthesiology medical specialty. No special flags apply to this device.

510(k) Clearances

24 matches
K Number
Device Name
MXR-2000 FLOWMETER
OHMEDA - LOW FLOW FLOWMETER
FR6000 FLOWMETER
SERIES D FLOWMETER
CLASSIC (TM) 200 OXYGEN FLOWMETER
AIRCO 2000 SERIES FLOWMETERS
SELECT FLOWMETER
OXYGEN DELIVERY MEASURING DEVICE
PRESSURE RELIEF ADAPTOR
FLOWMETER, BACKPRESSURE COMPENSATED, THORPE TUBE
RECON-2 FLOW CONTROLLER
PRESET FLOWMETER
TIMETER-PRODUCED PURITAN BENNETT AIR ADP
RECON 1
RESPIRATORY THERAPY FLOWMETER
MO8 OXYGEN FLOWMETER
M015 OXYGEN & MA15 AIR
MODEL 54 FLOWMETER BACK-PRESSURE TUBE
FLOWMETER, BACK PRESSURE COMPENSATED,
FLOW LIMITER
LINDE OXYGEN THERAPY FLOWMETERS, L33-L34
FLOMETER
FLOWMETER, OXYGEN
FLOWMETER, P.C., REDESIGNED VERSION

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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