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.
Let the assistant find your predicates
Describe your device and the Research Assistant searches 510(k)s, compares intended use, and drafts a predicate shortlist — with citations.
Free to try · every answer cites its records
Blood Collection Device For Cell-Free Nucleic Acid
Clinical Chemistry
The Blood Collection Device for Cell-Free Nucleic Acid is a medical device intended to collect, store, transport, and handle blood specimens while stabilizing and isolating cell-free nucleic acid components for subsequent testing, such as liquid biopsy assays. It is used in clinical laboratories to ensure the integrity of cell-free DNA or RNA prior to molecular analysis. This device is classified as FDA Class 2, requiring 510(k) clearance, under regulation 862.1676 in the Clinical Chemistry specialty. It carries product code QMA and is not an implant, not life-sustaining, and not GMP exempt.
510(k) Clearances
2 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.