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: BYL FDA class 1

Tent, Oxygen

Anesthesiology

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The Tent, Oxygen is a non-powered enclosure used to provide supplemental oxygen to patients, particularly children, by surrounding them with an oxygen-enriched environment. 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 BYL, regulated under 21 CFR 868.5700 in the Anesthesiology specialty.

510(k) Clearances

11 matches
K Number
Device Name
NASCOR IGLOO
NASCOR OXYDOME
SPAG PAK
DIRD INGANT O2 (BIO 2 HOOD)
KEYSTONE OXYGEN TENT
NOVA OXYGEN TENT
AEROSOL DELIVERY HOOD
MEDI-COMP NEONATAL OXYGEN HOOD
SEA-LONG NECKSEAL & HOOD
HOO2D SEAT-INFANT
MEDIUM SIZE OXYGEN HOOD #1547

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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