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: BZB FDA class 1

Catheter, Nasal, Oxygen

Anesthesiology

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The Catheter, Nasal, Oxygen is a flexible catheter inserted into a nostril and advanced into the nasopharynx to deliver supplemental oxygen directly to the upper airway for patients requiring low-to-moderate flow oxygen therapy. It is classified as FDA Class 1, the lowest risk category, subject to general controls only with no premarket submission required. The product code is BZB, regulated under 21 CFR 868.5350 in the Anesthesiology specialty.

510(k) Clearances

8 matches
K Number
Device Name
OXYGEN CATHETERS
PHARMA-PLAST OXYGEN CATHETER
DEMAND OXYGEN CONTROLLER
OXYGEN CATHETERS
NASAL OXYGEN CATHETER
OXYGEN CATHETER
CONPHAR OXYGEN CATHETER-STERILE
CATHETER, OXYGEN

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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