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: JJC FDA class 1

Analyzer, Chemistry (Sequential Multiple, Continuous Flow) Clinical Use

Clinical Chemistry

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This device is a sequential multiple continuous-flow chemistry analyzer used in clinical laboratories to perform automated, high-throughput measurement of multiple chemical analytes in patient specimens simultaneously, supporting diagnosis and monitoring of a wide range of conditions. It is classified as FDA Class 1, subject to general controls only with no premarket notification required. The product code is JJC, regulated under 21 CFR 862.2150, and assigned to the Clinical Chemistry medical specialty.

510(k) Clearances

32 matches
K Number
Device Name
AVL OMNI ANALYZER
NOVA 16 ANALYZER
OPERA SYSTEM
TECHNICON RA-2000(TM) SYSTEM
PARAMAX 520, PARAMAX 720 AND PARAMAX 720ZX
RFA/2 RAPID FLOW ANALYZER W/COMPUTER
AMRESCO FLOW PAC RANDOM ACCESS LIQUID #4901030
TECHNICON SMAC 3 SYSTEM
TECHNICON RA-XT(TM) SYSTEM IMMUNOASSAYS
TECHNICON RA-XT SYSTEM WITH ANALYTES
TECHNICON RA-500 SYSTEM
REPLACEMENT REAGENTS FOR SMAC II SYSTEMS
LANCER ANALYZER CUPS
TECHNICON RA-1000 SYSTEM
SBA 300 CLINICAL CHEMISTRY ANALYZER
TECHNICON RA 1000 SYSTEM
TECHNICON SMAC II SYSTEM & ACCESSORIES
PRE-VAP CAPS
BMC RIAFLO SYSTEM
NSI WASH SOLUTION CONCENTRATE
PHOTOVOLT PVA 4M+2 ANALYZER
TECHNICON C800 SYSTEM
TECHNICON STAT/LYTE ISE ELECTROLYTE
AUTOMATIC ANALYZER
SMA II
IN VITRO DIAGNOSTIC REAGENTS
SMA MICROLYZER
REAGENTS
SYSTEM 5 - SEMI-AUTOMATED CLIN. ANALY
MT II - TEST FOR CONTINUOUS FLOW ANAL
LANCER AUTOANALYZER MANIFOLD PUMP TUB
ANALYZER, GLUCOSE/UREA/CREATININE

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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