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.
Non-Coring (Huber) Needle
General Hospital
The Non-Coring (Huber) Needle is a specially designed needle with a deflected tip used to access subcutaneous implanted intravascular infusion ports without coring the port's septum, thereby preserving septum integrity for repeated use; it can also access other non-vascular implanted devices with similar septums. It is classified as FDA Class 2 under 21 CFR 880.5570 in the General Hospital specialty, requiring 510(k) premarket notification. Product code PTI; not an implant and not life-sustaining.
510(k) Clearances
12 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.