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.
Needle, Gastro-Urology, Reprocessed
General, Plastic Surgery
The gastro-urology needle (reprocessed) is a surgical needle used in gastrointestinal or urological procedures, such as tissue aspiration or injection in abdominal or pelvic organs. It is classified as FDA Class 1 under regulation 878.4800 in the General and Plastic Surgery specialty, subject to general controls without GMP exemption. Reprocessing validation data must be included in a 510(k) submission for this device. Product code NMU is eligible for third-party review.
No 510(k) clearances found for "NMU". Try a different K-number, product code, or device name.
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.