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: FRP FDA class 1

Holder, Infant Position

General Hospital

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An infant position holder is a device used to safely and securely position infants during clinical procedures or transport, reducing the risk of movement or injury. It is classified as FDA Class 1 (lowest risk), subject to general controls only, and does not require premarket notification. The product code is FRP, regulated under 21 CFR 880.5680, within the General Hospital medical specialty. This device is both exempt from GMP requirements and eligible for third-party 510(k) review.

510(k) Clearances

14 matches
K Number
Device Name
INFANT SLEEP BEANIE
RES-Q INFANT WEDGE AND SLING
KOZY COMFORT INFANT POSITIONER
HEAD BED
ROBIN HOOD VEST
NIGHTFORM
KENDALL-LTP TURNER SAVE-A-LINE
NEONATAL RESTRAINT AND COMFORT SYSTEMS
THE TUCKER SLING
PEDICRAFT INFANT REFLUX WEDGE
INFANT REFLUX SLING
CUDDLE UP PILLOW
PREMIE COMFORT PAD PATIENT & INFANT SUPPORT PADS
PEDIATRIC POSITION HOLDER

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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