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.
System, Fibrinogen Determination
Hematology
This device is a fibrinogen determination system, an in vitro diagnostic system used to measure plasma fibrinogen levels, an important coagulation factor, to assess bleeding risk and monitor conditions such as disseminated intravascular coagulation (DIC) and liver disease. It is classified as FDA Class 2, indicating moderate risk, and requires 510(k) premarket notification. The product code is KQJ, regulated under 21 CFR 864.7340 within the Hematology specialty. This device is eligible for third-party review.
510(k) Clearances
27 matchesWhat 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.