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: JAY FDA class 1

Support, Breathing Tube

Anesthesiology

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A breathing tube support is a device used to hold and stabilize endotracheal or tracheostomy tubes in proper position, preventing accidental dislodgement and reducing patient discomfort during airway management. It is classified as FDA Class 1, the lowest risk category, requiring only general controls and not subject to premarket notification requirements. The product code is JAY, regulated under 21 CFR 868.5280, within the Anesthesiology medical specialty. No special flags apply to this device.

510(k) Clearances

19 matches
K Number
Device Name
CUSTOM MEDICAL SUSPENSION STRAP
BLOCK, BITE, INTUBATION
DALE HEAD BAND ANESTHESIA CIRCUIT TUBE HOLDER 1315
JEE FRAME (VENTILATOR CIRCUIT SUPPORT)
COMFIT PLUS ENDOTRACHEAL TUBE HOLDER & BITE BLOCK
ENDO-SECURE
TRACH MATE
COMFIT
TUBE-TITLE
BITE-BLOCK
SCHULTZ ENDHOLD
DALE ENDOTRACHEAL TUBE HOLDER
ENDOTRACHEAL TUBE HOLDER
ADJUSTABLE TUBE TREE FOR ANESTH. HOSES
TUBE-STRAP
ADULT ZEE-FRAME
ZEE-FRAME
FLEX ARM BE 122, CLAMP 122-27
CLAMP BE-152

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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