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.

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Describe your device and the Research Assistant searches 510(k)s, compares intended use, and drafts a predicate shortlist — with citations.

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Product Code: DBI FDA class 2

Complement C4, Antigen, Antiserum, Control

Immunology

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This is an immunological reagent kit for detecting and measuring complement C4, a component activated in the classical and lectin pathways of the complement system and reduced in conditions such as systemic lupus erythematosus and hereditary C4 deficiency. The kit includes antigen, antiserum, and control components for in vitro diagnostic testing. It is classified as FDA Class 2, requiring 510(k) premarket notification, and is eligible for third-party review. The product code is DBI, regulated under 21 CFR 866.5240, within the Immunology specialty.

510(k) Clearances

34 matches
K Number
Device Name
SPAPLUS ANALYZER
TINA-QUANT COMPLEMENT C4 TEST SYSTEM
WAKO AUTOKIT C4
RANDOX COMPLEMENT C4
DIMENSION C4 FLEX REAGENT CARTRIDGE
C4 MININEPH ANTISERUM
K-ASSAY C4
C4
N-ASSAY TIA MULTI V-NL
N-ASSAY TIA C4 TEST KIT
OLYMPUS C4 IMMUNOTURBIDIMETRIC REAGENT
QUANTEX C4
IL TEST COMPLEMENT 4
RAICHEM SPIA C4 REAGENT
EZ COMPLEMENT C4
SPQ(TM) ANTIBODY REAGENT SET II FOR C4
COMPLEMENT C4 FOR THE TECHNICON DPA-1(TM) SYSTEM
QM300 C4 ANTIBODY PACK
PRECIMAT(R) C4
TINA-QUANT(R) (A) C4
QUANTIMETRIC PLUS C4 REAGENT KIT
GILFORD C4 COMPLEMENT REAGENT
SPQ TEST SYSTEM FOR COMPLEMENT C4
C4 ANTIGEN ANTIBODY CONTROL
RABBIT ANTISERUM TO HUMAN C4
FIAX COMPLEMENT C4 TEST KIT
IMMUNOGL. FRCT. OF RABBIT ANTISER.-C4
SCRIPPSYSTEM C4 RID KIT
GOAT ANTI-HUMAN COMPLEMENT C4
COMPLEMENT C4 NEPHELOMETRIC ASSAY
RADIAL IMMUNODIFFUSION KIT-COMP. 3
COMPLEMENT C4 NEPHELOMETRIC ASSAY
HUMAN C4 COMPLEMENT CONTROL SERUM
PLATES FOR HUMAN C4 COMPLEMENT

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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