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: DEB FDA class 2

Alpha-2-Macroglobulin, Antigen, Antiserum, Control

Immunology

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This is an immunological reagent kit for detecting alpha-2-macroglobulin, the major broad-spectrum protease inhibitor in plasma that neutralizes proteases by steric entrapment, including antigen, antiserum, and control components for standard immunoassay procedures in clinical laboratories. It is classified as FDA Class 2, indicating moderate risk, and requires 510(k) premarket notification. The product code is DEB, regulated under 21 CFR 866.5620, within the Immunology specialty.

510(k) Clearances

13 matches
K Number
Device Name
HUMAN ALPHA2-MACROGLOBULIN KIT FOR USE ON SPAPLUS
DIMENSION VISTA SYSTEM A2MAC FLEX REAGENT CARTRIDGE, DIMENSION VISTA SYSTEM PROTEIN 1 CALIBRATOR, DIMENSION VISTA SYSYEM
N ANTISERA TO HUMAN ALPHA2-MACROGLOBULIN
IMMAGE IMMUNOCHEMISTRY SYSTEM ALPHA-2-MACROGLOBULIN REAGENT
ALPHA-2 MACROGLOBULIN TEST RID KIT
QM300 ALPHA2 MACROGLOBULIN ANTIBODY PACK
72 DETERM. SIZE RADIAL IMMUNODIFFUSION TEST ALPHA2
RADIAL IMMUNODIFFUSION PLATES ALPHA-2 MACROGLOBULI
SPQ TEST SYSTEM FOR ALPHA(2) MACROGLOBULIN
IMMUNOGL. FRCT. OF RABBIT ANTISER.-MACRO
HUMAN ALPHA2 MACROGLOBULIN
ALPHA-2-MACROGLOBULIN NEPHEL. ASSAY
LAS-R TM

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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