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.
Diagnostic Ultrasonic Transducer, Robotic
Radiology
The Diagnostic Ultrasonic Transducer, Robotic (product code OQQ) is a robotic ultrasound transducer intended for diagnostic ultrasonic imaging or monitoring applications. It is designed to be used in robotic-assisted environments for non-invasive imaging of internal body structures. As an FDA Class 2 device under regulation 892.1570, it requires 510(k) premarket clearance and falls within the Radiology medical specialty. The device is eligible for third-party 510(k) review and is not an implant or life-sustaining device.
510(k) Clearances
1 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.