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: CIJ FDA class 2

Saccharogenic, Amylase

Clinical Chemistry

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The Saccharogenic, Amylase test system (product code CIJ) is an in-vitro diagnostic device used in clinical chemistry to measure amylase enzyme activity in serum or urine using a saccharogenic method that quantifies reducing sugars released from starch substrate, supporting the diagnosis of pancreatitis and salivary gland disorders. It is classified as FDA Class 2, indicating moderate risk, and requires a 510(k) premarket notification. It falls under regulation 21 CFR 862.1070 in the Clinical Chemistry medical specialty. This device is eligible for third-party review under the FDA's accredited persons program.

510(k) Clearances

31 matches
K Number
Device Name
AMYLASE EPS-G7 (LIQUID) REAGENT SET, (HITACHI ANALYZERS)
ADDITIONAL IMS ASSAYS FOR THE BAYER ADVIA IMS SYSTEM
AMYLASE
AMYLASE (ETHYLIDENE PNGPG7) KIT
AMYLASE TEST ITEM 97381/94 (R1, 97382/94 (R2-SR)
LIQUID AMYLASE (CNPG3) REAGENT SET
DMA AMYLASE (DEMAND) PROCEDURE
OLYMPUS AMYLASE REAGENT
BIOTROL AMYLASE CNPG3
-AMYLASE EPS
IL 35260, IL TEST AMYLASE REAGENT
ISOMUNE-AMYLASE AND ISOMUNE-AMYLASE CONTROL
BIOTROL ALPHA AMYLASE
D.A.T. (TM) AMYLASE REAGENT
AMYLASE REAGENT
AMYLASE,CALCIUM,CHLORIDE & TRIGLYCERIDES ON CHEM 1
DART AMYLASE-D.S. REAGENT SYSTEM
AMYLASE PROCEDURE
EMDS AMYLASE (AMYL) TEST PACKS, # 67653/95
ISOTRAK AMYLASE TEST AMYLASE ISOENZYME
X-AMYLASE ASSAY KIT
SYSTEMATE A AMYLASE HEM 67204
DART ALPHA-AMYLASE REAGENT SYSTEM
DADE COLORIMETRIC AMYLASE
ULTRA ZYME PLUS AMYL #64982 & 65031
CHEM-STRATE AMYLASE
SZAMYL 6.5
ULTRA ZYME PLUS AMYL 64982, GILFORD 3500
ULTRAZYME PLUS AMYL, CENTRIFICHEM APPLI.
ENZYMATIC AMYLASE REAGENT KIT
ULTRAZYME AMYLASE

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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