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.
Nucleic Acid Detection System For Non-Viral Microorganism(S) Causing Sexually Transmitted Infections
Microbiology
The Nucleic Acid Detection System For Non-Viral Microorganism(S) Causing Sexually Transmitted Infections is an in vitro diagnostic device intended for the detection and identification of nucleic acids from non-viral microorganisms in clinical specimens from patients suspected of sexually transmitted infections, used as an aid to diagnosis in conjunction with other clinical and laboratory data. It is classified as FDA Class 2, requiring 510(k) premarket notification under regulation 866.3393 in the Microbiology specialty. The product code is QEP. It is not an implant and is not life-sustaining.
510(k) Clearances
20 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.