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: LKP FDA class 2

Anti-Sm Antibody, Antigen And Control

Immunology

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Anti-Sm Antibody, Antigen and Control is a diagnostic immunoassay system used to detect antibodies against the Smith (Sm) antigen, a nuclear antigen that is highly specific for systemic lupus erythematosus (SLE) and is used as a confirmatory marker for that condition. It is classified as FDA Class 2, indicating moderate risk, and requires 510(k) premarket clearance. The product code is LKP, regulated under 21 CFR 866.5100, within the Immunology medical specialty. This device is eligible for third-party 510(k) review.

510(k) Clearances

28 matches
K Number
Device Name
EliA SmDP-S
EliA SmDP Immunoassay
EIA SMDP IMMUNOASSAY
QUANTA FLASH SM, QUANTA FLASH RNP, QUANTA FLASH SM CALIBRATORS, QUANTA FLASH RNP CALIBRATORS, QUANTA FLASH SM CONTROLS,
THERATEST EL-ANA PROFILES
VARELISA SM ANTIBODIES, MODEL 18296
LIQUICHEK ANTI-SM CONTROL, POSITIVE, CATALOG #115
FRED HUTCHINSON CANCER RESEARCH CENTER ENZYME ANTI-SR PROTEIN ANTIBODY TEST
RHIGENE MESACUP2 TEST- SM
VARELISA SM ANTIBODIES
AUTOSTAT II ANTI-SM ELISA
LIQUICHEK ANTI-SM CONTROL, EIA, MODEL 208
THE APTUS(AUTOMATED)APPLICATION OF THE SM ELISA TEST SYSTEM.AN ENZYME LINK IMMUNOSORBENT ASSAY(ELISA)FOR THE DETECTIOO
SERAQUEST ANTI-SM
SERAQUEST ANTI-SM/RNP
ORGENTEC ANTI-SM(SMITH) PIN IMMUNO ASSAY
HYTEC AUTOIMMUNE KITS (SM)
ENZYME IMMUNOASSAY ANTI-SM ANTIBODY TEST KIT
SYNELISA SM ABS/RNP-SM ABS
IMMUNOWELL RNP/SM ANTIBODY TEST
IMMUNOWELL SM ANTIBODY TEST
DIASTAT ANTI-SM/RNP
DIASTAT ANTI-SM
RHEUMELISA ASSAY FOR SM AUTOANTIBODIES
WESBLOT RNP-SM TEST
SM ANTIBODY TEST KIT
IMMUSTRIP(TM) SM ELISA TEST SYSTEM
ENZYMATIC ACETAMINOPHEN ASSAY

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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