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: FPY FDA class 1

Sheet, Burn

General Hospital

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The Burn Sheet is a sterile or non-sterile covering applied to large burn areas on a patient's body to protect the wound from contamination, reduce fluid loss, and provide comfort during emergency treatment and transport. It is classified as FDA Class 1 (lowest risk) and is subject only to general controls. The product code is FPY, regulated under 21 CFR 880.5180 in the General Hospital specialty.

510(k) Clearances

17 matches
K Number
Device Name
CP & S STERILE BURN SHEET
BURNSHIELD FIRE BLANKET
BURNSHIELD TRAUMA DRESSING
BURN SHEET
BURNS CASUALTY SHEET
BURNS CASUALTY SHEET LIMB WRAP
BURNS CASUALTY SHEET BURN ROLL
LYOSHEET SURGICAL SHEET FOR BURNS
KENDALL CURITY BURN PAD
FIRST RESPONSE EMERG. MEDICSL - BURNS
ABSORB FURN SHEET
WATER JEL FIRE BLANKET
TEMPORARY BURN SHEET WITH PERFORATED
TEMPORARY BURN SHEET WITH PERFORATED
BURN DRESSING PAD
BLANKET, WATER-JEL FIRE
BLANKET, BURN

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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