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.

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Describe your device and the Research Assistant searches 510(k)s, compares intended use, and drafts a predicate shortlist — with citations.

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Product Code: JFM FDA class 2

Enzymatic Method, Bilirubin

Clinical Chemistry

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Enzymatic Method for Bilirubin is a clinical chemistry test system that uses enzymatic reactions to measure bilirubin concentration in serum or plasma, used in the diagnosis and monitoring of liver disease, hemolytic disorders, and neonatal jaundice. It is classified as FDA Class 2 (moderate risk), subject to general and special controls, and requires 510(k) premarket notification. The product code is JFM, regulated under 21 CFR 862.1110, within the Clinical Chemistry medical specialty. This device is eligible for third-party 510(k) review.

510(k) Clearances

11 matches
K Number
Device Name
ADVIA® Chemistry Total Bilirubin_2 (TBIL_2)
Direct Bilirubin
Total Bilirubin
ADVIA CHEMISTRY TOTAL BILIRUBIN_2
WAKO DIRECT BILIRUBIN V, MODELS 996-23591, 412-22901, 992-23691, 998-23791
WAKO TOTAL BILIRUBIN V, MODELS 410-22701, 998-23291, 416-22801, 990-23191
DRI-STAT ENZYMATIC BILIRUBIN REAGENT, SYNCHRON SYSTEMS BILIRUBIN CALIBRATOR
DIRECT BILIRUBIN LIQUICOLOR AND TOTAL BILIRUBIN LIQUICOLOR
WAKO TOTAL BILIRUBIN V
ENZYMATIC BILIRUBIN (TOTAL), CATALOGUE NO. 202-14
DRI-STAT ENZYMATIC BILIRUBIN TEST KIT

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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