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.
Radioimmunoassay, Tricyclic Antidepressant Drugs
Clinical Toxicology
A radioimmunoassay for tricyclic antidepressant drugs is a laboratory test intended to measure any of the tricyclic antidepressant drugs in serum or urine, used for therapeutic drug monitoring or toxicological screening in clinical and forensic settings. The device is FDA Class 2, indicating moderate risk and requiring 510(k) premarket clearance. It carries product code LFG and is regulated under 21 CFR 862.3910 within the Clinical Toxicology specialty. This device is eligible for third-party review.
510(k) Clearances
21 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.