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.
Stimulator, Nerve, Electrical, Transcutaneous, Limited Output, Arthritis Pain Relief
Neurology
The Limited Output Transcutaneous Electrical Nerve Stimulator for Arthritis Pain Relief (product code OCF) is a neurological device that delivers electrical stimulation to nerves for relief of pain associated with arthritis, including both osteoarthritis and rheumatoid arthritis. The device is transcutaneous (applied to the skin surface) and is designed with a limited output to ensure safe stimulation levels. This device is FDA Class 2 under regulation 882.5890 in the Neurology specialty, requires 510(k) clearance, and is eligible for third-party review. It carries no implant or life-sustaining flags.
510(k) Clearances
1 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.