Tool · 510(k)

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.

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Describe your device and the Research Assistant searches 510(k)s, compares intended use, and drafts a predicate shortlist — with citations.

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Product Code: QKZ FDA class 2

Magnetically Maneuvered Capsule Endoscopy System

Gastroenterology, Urology

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The Magnetically Maneuvered Capsule Endoscopy System is a Class 2 gastroenterology device consisting of an ingestible capsule and magnetic controller used for visualization of the stomach and duodenum; the capsule contains a wireless camera while an external magnetic controller is magnetically coupled with the capsule to control its location and viewing direction. It requires 510(k) clearance and is regulated under 21 CFR 876.1310 within the Gastroenterology and Urology medical specialty. The product code is QKZ. The device is not an implant and is not flagged as life-sustaining.

510(k) Clearances

6 matches
K Number
Device Name
NaviCam Xpress Stomach Capsule Endoscope System (NaviCam Xpress Stomach System) with NaviCam Stomach Capsule/Tether (NaviCam Xpress Stomach System with NaviCam Capsule/Tether)
NaviCam Xpress Stomach Capsule Endoscope System (NaviCam Xpress Stomach System) with NaviCam Capsule and NaviCam Tether
NaviCam Xpress Stomach System, NaviCam Xpress System
NaviCam Capsule Endoscope System with NaviCam Stomach Capsule and NaviCam Tether, NaviCam Xpress Stomach Capsule Endoscope System (NaviCam Xpress Stomach System) with NaviCam Stomach Capsule and NaviCam Tether
NaviCam Xpress Stomach System
NaviCam Capsule Endoscope System with NaviCam Stomach Capsule

What 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.

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