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: LIG FDA class 2

Radioassay, Intrinsic Factor Blocking Antibody

Clinical Chemistry

View full classification →

A radioassay for intrinsic factor blocking antibody is a laboratory test that uses radiolabeled reagents to detect antibodies that block the binding of vitamin B12 to intrinsic factor in patient serum, used in the diagnosis of pernicious anemia and other autoimmune conditions affecting vitamin B12 absorption. The device is FDA Class 2, indicating moderate risk and requiring 510(k) premarket clearance. It carries product code LIG and is regulated under 21 CFR 862.1810 within the Clinical Chemistry specialty. This device is eligible for third-party review.

510(k) Clearances

8 matches
K Number
Device Name
Access Intrinsic Factor Ab
IMMULISA INTRINSIC FACTOR ANTIBODY ELISA
QUANTA LITE INTRINSIC FACTOR ELISA
INSTRINSIC FACTOR AB, CALIBRATORS, AND QC ON THE ACCESS IMMUNOASSAY SYSTEMS, MODELS 387992, 387993, 387999
IMMULITE 2000 VITAMIN B12, MODEL L2KVB2, L2KVB6
ABBOTT ARCHITECT B12
IMX B12
1F BLOCKING ANTIBODY(57 CO) RADIOASSAY

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.

Popular Product Codes

Commonly searched