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: MPO FDA class 1

Infant Heel Warmer (Chemical Heat Pack)

Physical Medicine

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The Infant Heel Warmer (Chemical Heat Pack) is a physical medicine device used to warm the heel of neonates and infants prior to heel-stick blood collection procedures, increasing blood flow to facilitate sample collection. Classified as FDA Class 1 under 21 CFR 890.5710 in the Physical Medicine specialty, it requires 510(k) notification and is eligible for third-party review. The product code is MPO.

510(k) Clearances

11 matches
K Number
Device Name
Infant Heel WarmerTM; Heel Snuggler®
Infant Heel Warmer (Model 24401) and WarmGel Infant Heel Warmer (Model 20418)
Rapid Aid Instant Disposable Infant Heel Warmer
DENOVO TEDDY GEL INFANT HEEL WARMER
INFANT HEEL WARMER BY INTCO
RAPID AID INSTANT DISPOSABLE INFANT HEEL WARMER
HEEL SNUGGLER, MODEL 99047
MEDI-HEAT INFANT HEEL WARMER
RECOVER INFANT HEEL WARMER (5100)
BAXTER SODIUM ACETATE INFANT HEEL WARMER
DEROYAL INDUSTRIES INFANT HEEL WARMER

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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