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: LDY FDA class 1

Fixative, Formalin-Containing

Pathology

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A formalin-containing fixative is a widely used pathology reagent in which formaldehyde in aqueous solution preserves biological tissue specimens by cross-linking proteins, maintaining tissue architecture for histological examination and diagnostic interpretation. It is classified as FDA Class 1, subject only to general controls, and is exempt from Good Manufacturing Practice (GMP) requirements. The product code is LDY, regulated under 21 CFR 864.4010, in the Pathology specialty. No premarket notification is required.

510(k) Clearances

1 matches
K Number
Device Name
DIACYTE FIXATIVE SOLUTION

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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