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.
Sampler, Amniotic Fluid (Amniocentesis Tray)
Obstetrics/Gynecology
The Amniotic Fluid Sampler, also known as an amniocentesis tray, is a collection of instruments used to obtain amniotic fluid from the uterus during pregnancy for prenatal diagnostic testing, such as chromosomal or genetic analysis. It is classified as FDA Class 1, meaning it presents the lowest level of risk and is subject only to general controls such as labeling, registration, and good manufacturing practices. The product code is HIO, regulated under 21 CFR 884.1550, within the Obstetrics/Gynecology medical specialty. No special risk flags apply to this device.
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.