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: LJM FDA class 2

Antinuclear Antibody (Enzyme-Labeled), Antigen, Controls

Immunology

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Antinuclear Antibody (Enzyme-Labeled), Antigen, Controls are enzyme-labeled antigens and control materials used in immunoassay systems to detect antinuclear antibodies (ANA), which are markers associated with autoimmune conditions such as systemic lupus erythematosus. It is classified as FDA Class 2, indicating moderate risk, and requires 510(k) premarket clearance. The product code is LJM, regulated under 21 CFR 866.5100, and is reviewed within the Immunology specialty. This device is eligible for third-party 510(k) review.

510(k) Clearances

50+ matches
K Number
Device Name
EliA CENP Immunoassay, EliA U1RNP Immunoassay, EliA RNP70 Immunoassay
ImmuLisa Enhanced Centromere Antibody ELISA
ELIA SCL-70S IMMUNOASSAY
QUANTA FLASH CENTROMERE
GOLD STANDARD DIAGNOSTICS ANTI-NUCLEAR ANTIBODY (ANA) SCREEN ELISA TEST KIT
ANA SCREEN ELISA (IGG)
VARELISA RECOMBI ANA SCREEN, MODEL 12 596
VARELISA RECOMBI CTD SCREEN, MODEL 13096
VARELISA RECOMBI ANA PROFILE, MODEL 18496
IMMULISA ANTINUCLEAR ANTIBODY SCREEN ELISA
AESKULISA ANA HEP-2
VARELISA HISTONE ANTIBODIES, MODEL 16496
EL-ANA PROFILES: ANTI-CHROMATIN
MESACUP-2 TEST CENP-B
ANA DETECT
THE THERATEST EL-ANA PROFILES: ANTI-CENTROMERE
RHIGENE ANA ELISA TEST SYSTEM, MODEL K7560
ANA EIA DIAGNOSTIC TEST KIT
QUANTA LITE CENTROMERE (CENP-A & CENP-B) ELISA
EL-ANA PROFILES-2K1
THE APTUS (AUTOMATED) APPLICATION OF THE TG IGG ELISA TEST SYSTEM. AN ENZYME LINKED IMMUNOSORBENT ASSAY (ELISA) FOR THE
THE APTUS (AUTOMATED APPLICATION OF THE TPO IGG ELISA TEST SYSTEM. AN ENZYME LINKED IMMUNOSORBENT ASSAY (ELISA) FOR THE
MDI SCL-70 TEST
RHIGENE ANA ELISA TEST SYSTEM
MDI SM/RNP TEST
MDI SS-A TEST
VARELISA RECOMBI ANA PROFILE
VARELISA RECOMBI ANA SCREEN EIA, MODELS 128 48/ 128 96
RELISA ANA SCREENING TEST SYSTEM, MODEL 7096-11
AUTOSTAT II ANA SCREEN ELISA
THE APTUS (AUTOMATED) APPLICATION OF THE ANA SCREEN ELISA TEST SYSTEM. AN ENZYME LINKED IMMUNOSORBENT ASSAY (ELISA) FOR.
DIAMEDIX IMMUNOSIMPLICITY ANA (IS-ANA) SCREEN TEST SYSTEM
SERAQUEST ANTI-SSA
ELIAS ANA-HEP-2
HY-TEC/MANUAL AUTOIMMUNE KIT FOR HISTONE
ORGENTEC ANTI-SM ELISA
ORGENTEC ANTI-RNP/SM ELISA
ORGENTEC ABTI-SS-BB(LA) ELISA
ORGENTEC ANTI-JO-1 ELISA
ORGENTEC ANTI-SCL 70 ELISA
ORGENTEC ANTI-SS-A(RO) ELISA
VARELISA ANA (4) PROFILE
ORGENTEC ANTI-JO-1 PIN IMMUNO ASSAY
ORGENTEC ANTI-SS-B(LA) PIN IMMUNO ASSAY
ORGENTEC ANTI-SCL 70 PIN IMMUNO ASSAY
ORGENTEC ANTI-SS-A(RO) PIN IMMUNO ASSAY
THERATEST KIT (MODIFICATION)
QUANTA LITE SSDNA
IMAGETITER INSTRUMENT, ANA TEST KIT & CALIBRATOR SERUM
THERATEST LAB, INC., EL-ANASCR KIT

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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