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: CJE FDA class 2

Nitrophenylphosphate, Alkaline Phosphatase Or Isoenzymes

Clinical Chemistry

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The Nitrophenylphosphate, Alkaline Phosphatase or Isoenzymes test system (product code CJE) is an in-vitro diagnostic device used in clinical chemistry to measure alkaline phosphatase activity or its isoenzymes in serum using para-nitrophenyl phosphate as a chromogenic substrate, a standard photometric method widely used in automated clinical analyzers. It is classified as FDA Class 2, indicating moderate risk, and requires a 510(k) premarket notification. It falls under regulation 21 CFR 862.1050 in the Clinical Chemistry medical specialty. This device is eligible for third-party review under the FDA's accredited persons program.

510(k) Clearances

50+ matches
K Number
Device Name
Alkaline Phosphatase
Alkaline Phosphatase2
Yumizen C1200 ALP, Yumizen C1200 Albumin
Comprehensive Metabolic Panel, skyla Clinical Chemistry Analyzer, Minicare C300 Clinical Chemistry Analyzer
ALP IFCC Gen.2
Randox RX Daytona Plus Alkaline Phosphatase (ALP)
ACE ALKALINE PHOSPHATASE REAGENT, AMYLASE REAGENT, ALT REAGENT, AST REAGENT
S TEST REAGENT CARTRIDGE ALP (ALKALINE PHOSPHATASE)
ACE ALKALINE PHOSPHATASE REAGENT, ACE AMYLASE REAGENT, ACE LDH-L REAGENT
ELITTECH CLINICAL SYSTEMS ALP IFCC SL
EASYRA ALKALINE PHOSPHATASE, ASPARTATE AMINOTRANSFERASE AND AMYLASE REAGENTS
ALKALINE PHOSPHATASE (IFCC) PLUS, ECAL, NORTROL, ABTROL
GENERAL CHEMISTRIES ON ABX PENTRA 400 CLINICAL CHEMISTRY ANALYZER
COBAS INTEGRA ALP IFCC GEN.2
MODIFICATION TO ALKP
WIENER LAB. ALP 405
TRACE SCIENTIFIC ALKALINE PHOSPHATASE, TWO PART LIQUID, MODEL TR-113
ALKALINE PHOSPHATASE LIQUID REAGENT
ALKALINE PHOSPHATASE-SL ASSAY, MODELS 328-17 AND 328-30
ATAC PAK ALP REAGENT KIT
ALKALINE PHOSPHATASE LIQUID REAGENT-KINETIC, MODELS A504-150 AND A504-500H
ALKALINE PHOPHATASE (ALP), PRODUCT NO'S 118-01, 118-02
ELAN ALKALINE PHOSPHATE REAGENT KIT
CARESIDE ALKALINE PHOSPHATASE
ROCHE COBAS INTEGRA ALKALINE PHOSPHATASE IFCC LIQUID REAGENT CASSETTE, ROCHE COBAS INTEGRA PANCREATIC A-AMYLASE EPS REAE
ALKP
ALKALINE PHOSPHATASE (ALKP)
ALKALINE PHOSPHATASE-SL ASSAY CATALOGUE NUMBER 309-10, 309-30
LIQUID ALKALINE PHOSHATASE REAGENT SET
ALP REAGENT SET
ALKALINE PHOSPHATASE
ALKALINE PHOSPHATASE (ALP) PROCEDURE NO. 245
ALKALINE PHOSPHATASE REAGENT SYSTEM
ALKALINE PHOSPHATASE (ALP/AMP) PROCEDURE NO. 247
ALKALINE PHOSPHATASE (ALKP) QVET
STANBIO ALKALINE PHOSPHATASE (LIQUICOLOR) TEST SET
EMDS ALKANINE PHOSPHATASE (ALP) TEST
AMP ALKALINE PHOSPHATASE REAGENT KIT
ALKALINE PHOSPHATASE KIT
OLYMPUS ALKALINE PHOSPHATASE REAGENT
EMDS ALKALINE PHOSPHATASE (ALP) TEST
OLYMPUS ALKALINE PHOSPHATASE REAGENT
ABBOTT QUICKSTART ALKA PHOSPHATASE (ALP) ITEM#5A38
SYSTEMATE ALKALINE PHOSPHATASE(EPOS APPL) #65483
KINETIC ALKALINE PHOSPHATASE DETERMINATION
ALKALINE PHOSPHATASE
SYNERMED ALKALINE PHOSPHATASE REAGENT KIT
ROCHE COBAS READY ALKALINE PHOSPHATASE REAGENT
AMRESCO ALKALINE PHOSPHATASE REAGENTS 7780 & 7781
COULTER ALP (ALK PHOS) REAGENT

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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