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: JJN FDA class 1

Apparatus, Electrophoresis, For Clinical Use

Clinical Chemistry

View full classification →

This device is an electrophoresis apparatus used in clinical laboratories to separate proteins, nucleic acids, or other charged biomolecules within patient specimens by applying an electric field, enabling identification of abnormal protein patterns associated with conditions such as multiple myeloma or hemoglobinopathies. It is classified as FDA Class 1 and is subject only to general regulatory controls with no premarket notification required. The product code is JJN, regulated under 21 CFR 862.2485, and belongs to the Clinical Chemistry medical specialty.

510(k) Clearances

34 matches
K Number
Device Name
POWER SUPPLY
ELECTROPHORESIS TANK
ELECTR-TRANSBLOTTER
REP SP ELECTROPHORESIS SYSTEM CAT NO. 3170
HELENA REP GEL PROCESSOR
RAPID ELECTROPHORESIS SYSTEM (REP)
STAVIP 3000
ELECTROPHORESIS WORK CENTER (EWC)
ISOGEL AGAROSE
EUROCHIMA SERUM PROTEIN ELECTROPHORESIS METHOD
OPTIPHOR-10
OPTICLEAR
ELVI 70 SAFETY CHAMBER
ELVI 18
IMMOBILINE SYSTEM LKB 1819
SARTOPHOR SYSTEM FOR ELECTROPHORESIS
CELLULOSE ACETATE MEMBRANE STRIPS
TITAN GEL HIGH RESOLUTION SERUM PROTEIN
TITANAN GEL SERUM PROTEIN ELECTROPHORES
HI-PHORE HIGH RESOLUTION ELECTROPHORES
AUTOMATED ELECTROPHORESIS SYSTEM
SPECIAL PROCEDURE AQAROSE FILM
GENERAL PROCEDURE AGAROSE FILM
CORNING 60 VOLT POWER SUPPLY
HIPP BUFFER(NON-BARBITAL), P/N
AGAROSE BARBITAL BUFFER
AGAROSE BARBITAL-EDTA BUFFER
BUFFERIZER
AUTOMATED ELECTROPHORESES MACHINE
CYSTIC FIBROSIS TESTING INSTRUMENT
ELECTROPHORESIS POWER SUPPLY TESTER
ELECTROPHORESIS OVEN THERMOMETER
ELECTROPHORESIS ACCESSORY MO. 3526
AGARO-GEL, PRODUCT # A1266

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.

Popular Product Codes

Commonly searched