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: JJQ FDA class 1

Colorimeter, Photometer, Spectrophotometer For Clinical Use

Clinical Chemistry

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This device is a colorimeter, photometer, or spectrophotometer intended for clinical laboratory use to measure the absorbance or transmittance of light by patient specimens or reaction products, enabling quantitative determination of biochemical analytes based on color intensity. It is classified as FDA Class 1 and is subject only to general controls with no premarket notification required. The product code is JJQ, regulated under 21 CFR 862.2300, and assigned to the Clinical Chemistry medical specialty.

510(k) Clearances

50+ matches
K Number
Device Name
UBIT-IR300 INFRARED SPECTROMETRY SYSTEM
DIGENE DML 2000 MICROPLATE LUMINOMETER
ALPHA 4 LS AUTOMATED MICROTITERPLATE PROCESSOR AND READER
STAT TRACKS
ANTHOS PHACTS VERSION MICROPLATE READER
CBI 7520 READER
ORIGEN ANALYZER
ANTHOS 2010 READER
ELX808 AUTOMATED MICROPLATE READERS
ELX800UV
BILI-METER
5STRATEC SL 300 LIA-MAT
DIGENE DCR-1 LUMINOMETER
WHITSOFT
BIOWHITTAKER CARTRIDGE SOFTWARE FOR EIA-400 PLATE READER
BIOWHITTAKER 2001 MICROPLATE READER FIRMWARE
ELX800 AND EL800 AUTOMATED MICROPLATE READERS
CERES 900C & CERES UV900C
PLATO 3300/1300
MICROREADER 4
SERUM/URINE APPLI ILAB(TM) CLINICAL CHEMISTRY SYSTEM
DUPONT ACA STAR
MRX MICROPLATE READER
BOEHRINGER MANNHEIM ES 300 AL(AUTOLOADER) ANALYZER
ILAB 900/1800 CLINICAL CHEMISTRY SYSTEM
ACCULYTE CHEMILUMINESCENCE ANALYZER
ANTHOS HT READERS, INCLUDING THE ANTHOS HT II&III
OMNI
OLYMPUS REPLY CLINICAL CHEMISTRY ANALYZER
LYRIS 100/120 LABORATORY INFORMATION SYSTEM
TECHNICON CHEM 1(R)/CHEM 1+(TM) SOFTWARE VER 11.1
LUMICO ANALYZER SA-300
BERTHOLD LB 954
LB 9502- CLINILUMAT, LB 953 - AUTO-CLIMILUMAT
MICROLITE MICROTITER PLATE LUMINOMETER ML3000
LABOTECH AUTOMATED MICROTITER ANALYZER
COBAS CORE IMMUNOCHEMISTRY SYSTEM
MICROLITE MICROTITER PLATE LUMINOMETER ML2250/MODI
SLT 340 ATTC
SLT SPECTRA
MP/S SINGLE WAVELENGTH MINI PHOTOMETER
ENCORE
AMERLITE PROCESSING CENTER
AUTO EIA MICROPLATE READ MODEL CERES 900 W/VAR OPT
MICROLITE ML 1000 MICROTITER PLATE LUMINOMETER
BARTELS PRIMA SYSTEM ADVANCED SCREENING CARTRIDGE
MICROTAK PLUS
OPUS(R) PLUS ANALYZER
IMX SELECT ANALYZER
METROLAB MODEL 1500

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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