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: DHN FDA class 2

Antinuclear Antibody, Indirect Immunofluorescent, Antigen, Control

Immunology

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The Antinuclear Antibody Indirect Immunofluorescent Antigen and Control is a diagnostic reagent used in indirect immunofluorescence assays to detect antinuclear antibodies (ANA) in patient serum, which are markers associated with autoimmune diseases such as lupus, Sjogren's syndrome, and rheumatoid arthritis. It is classified as FDA Class 2, requiring 510(k) premarket notification, and is regulated under 21 CFR 866.5100 within the Immunology specialty. The device is eligible for third-party 510(k) review.

510(k) Clearances

50+ matches
K Number
Device Name
Zeus IFA ANA HEp-2 Test System, Zeus dIFine
ImmuGlo HEp-2 Elite IFA
AESKUSLIDES ANA HEp-2-Gamma, HELIOS FULLY AUTOMATED IFA SYSTEM
Image Navigator by Immuno Concepts
EUROIMMUN IFA 40: HEP-20-10; EUROPATTERN MICROSCOPE AND SOFTWARE
NOVA Lite DAPI ANA Kit
IFA 40: HEP-20-10
AESKUSLIDES ANA HEP-2
EUROIMMUN ANA IFA: HEP-20-10
RHIGENE HEP-ANA TEST SYSTEM
LIQUICHEK AUTOIMMUNE NEGATIVE CONTROL, CATALOG #130
LIQUICHEK ANTI-SMOOTH MUSCLE CONTROL, POSITIVE, CATALOG #129
LIQUICHEK ANA CONTROL, SPECKLED PATTERN, POSITIVE, CATALOG #108
LIQUICHEK ANA CONTROL, NUCLEOLAR PATTERN, POSITIVE, CATALOG #111
LIQUICHEK ANTI-NDNA CONTROL, POSITIVE, CATALOG #119
LIQUICHEK ANTI-MITOCHONDRIAL CONTROL, POSITIVE, CATALOG #127
LIQUICHEK ANA CONTROL CENTROMERE PATTERN, POSITIVE, CATALOG #112
LIQUICHEK ANA CONTROL HOMOGENEOUS PATTERN CONTROL, POSOTIVE, CATALOG #118
LIQUICHEK ANA CONTROL SET, POSITIVE: HOMOGENEOUS, SPECKLED, CENTROMERE AND NUCLEOLAR PATTERNS, CATALOG #131
LIQUICHEK ANTI-MITOTIC SPINDLE PATTERN CONTROL, POSITIVE, CATALOG #118
VISIQUANT ANTI-NUCLEAR ANTIBODY TEST SYSTEM
HYPERION VISIQUANT ANA TEST KIT
POLYTITER SYSTEM
HEP-2 ANA TEST SYSTEM WITH IF-AIM TECHNOLOGY
INDIRECT FLUORESCENCE ASSAY FOR ANTI-NUCLEAR ANTIBODIES IGG ANTIBODY
LIQUICHEK ANA CONTROL, SPECKLED PATTERN, MODEL 202
LIQUICHEK ANA CONTROL, NUCLEOLAR PATTERN, MODEL 204
HEP-2000 COLORZYME ANA-RO TEST SYSTEM, MODEL 4200-RO
LIQUICHEK ANA CONTROL, CENTROMERE PATTERN, MODEL 203
LIQUICHEK ANA CONTROL, HOMOGENEOUS PATTERN, MODEL 201
HEP-2000 FLUORESCENT ANA-RO TEST SYSTEM
IFA HEP2 KIT FOR THE DETECTION OF ANTINUCLEAR ANTIBODIES
MICRO21 WITH NDNA
HEMAGEN ENA DSDNA KIT (EIA METHOD)
HEP-2000 COLORZYME ANA-RO TEST SYSTEM
HEP-2000 FLUORESCENT ANA-RO TEST SYSTEM
HEP-2 ANTINUCLEAR ANTIBODY TEST SYSTEM
DIASTAT ANTI-JO-1 KIT
HEMAGEN ENA [JO-I] KIT
NOVA LITE(TM) ANA KSL
NOVA LITE(TM) ANA MK
ANTINUCLEAR ANTIBODY (ANA) TEST SYSTEM
ANA ANTISERA CONTROL KIT
ANTI-NATIVE DNA ANTIBODY TEST (CRITHIDIA LUCILIAE)
NOVA LITE(TM) DSDNA
COMBIGENE(TM) ANTI-DNA #KADDZ, KADD1
BION ANTINUCLEAR ANTIBODY(ANA)TEST KIT/CONTR SERUM
ANTI-DNP MICROASSAY
CYTOTECH ANTINUCLEAR ANTIBODY (ANA) IFA KIT
TANGENT SYSTEM(TM) ANA PROFILE TEST 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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