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.
Theophylline Control Materials
Clinical Toxicology
Theophylline control materials are reference standards used in clinical toxicology laboratories to verify the accuracy and precision of theophylline assay systems, which measure blood levels of the bronchodilator theophylline. The device is classified as FDA Class 1, meaning it presents the lowest level of risk and requires only general regulatory controls without premarket notification. The product code is LAW, regulated under 21 CFR 862.3280, in the Clinical Toxicology specialty. No special flags apply.
510(k) Clearances
4 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.