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: CAM FDA class 1

Yoke Assembly, Medical Gas

Anesthesiology

View full classification →

The Medical Gas Yoke Assembly is a mechanical connector used in anesthesiology to attach a compressed gas cylinder to an anesthesia machine or gas delivery system, providing a secure, standardized interface that ensures proper connection and prevents cross-connection of gas supplies. It is classified as FDA Class 1 (lowest risk), subject only to general controls, and is exempt from premarket notification. The product code is CAM, regulated under 21 CFR 868.6885, within the Anesthesiology medical specialty. No special flags apply to this device.

510(k) Clearances

8 matches
K Number
Device Name
YOKE ASSEMBLY MEDICAL GAS
T-HANDLE ADAPTER, U-HANDLE & L HANDLER ADAPTER
PENOX DUAL FLOW MINIFOLD
FILL HOSE SAFETY ADAPTER
PENOX DUAL FEED MANIFOLD
GAS SUPPLY MANIFOLD SIEMENS-ELEMA AB
OXYGEN/NITROUS OXIDE OUTLET
OXYGEN MANIFOLD SYSTEMS, NITROUS OXIDE

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.

Popular Product Codes

Commonly searched