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.

Product Code: NEZ FDA class 2

System, Imaging, Gastrointestinal, Wireless, Capsule

Gastroenterology, Urology

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The System, Imaging, Gastrointestinal, Wireless, Capsule (product code NEZ) is a swallowable wireless capsule endoscopy system that captures images or video of the gastrointestinal tract as it passes through, enabling visualization of areas difficult to reach with conventional endoscopy. It is classified as an FDA Class 2 device within the Gastroenterology and Urology specialty, requiring 510(k) premarket clearance. No specific regulation number has been assigned to this product code. The device is not flagged as a permanent implant or life-sustaining device.

510(k) Clearances

45 matches
K Number
Device Name
CapsoCam Plus (SV-3) Capsule Endoscopy System
PillCam™ Genius SB System with PillCam Software v9.7 and PillCam Cloud Reader Software
NaviCam Small Bowel Capsule Endoscopy System with NaviCam SB Capsule and NaviCam Tether
PillCam SB 3 capsule endoscopy system, PillCam Software 9.0E
NaviCam Small Bowel Capsule Endoscopy System
PillCam SB 3 capsule endoscopy system, PillCam Software 9.0E
CapsoCam Plus (SV-3) Capsule Endoscopy System
CapsoCam Plus (SV-3)
Olympus Small Intestinal Capsule Endoscope System
MiroCam Capsule Endoscope System
Olympus Small Intestinal Capsule Endoscope System
MiroCam Capsule Endoscope System
PillCam SBC capsule endoscopy system, PilCam Desktop Software 9.0
RAPID Web
AdvanCE capsule endoscope delivery device
OLYMPUS SMALL INTESTINAL CAPSULE ENDOSCOPE SYSTEM
CapsoCam Plus (SV-3) Capsule Endoscope System
CapsoCam (SV-1)
MiroCam Capsule Endoscope System
ENDOCAPSULE SOFTWARE 10; ENDOCAPSULE SOFTWARE 10 LIGHT
GIVEN PILLCAM UGI CAPSULE ENDOSCOPY SYSTEM
MIROCAM CAPSULE ENDOSCOPE SYSTEM
MIROCAM CAPSULE ENDOSCOPE SYSTEM
GIVEN PILLCAM ENDOSCOPY SYSTEM WITH RAPID 8.0, GIVEN PILLCAM SB 3 CAPSULE ENDOSCOPY SYSTEM
MIROCAM CAPSULE ENDOSCOPE SYSTEM
OLYMPUS SMALL INTESTINAL CAPSULE ENDOSCOPE SYSTEM
MIROCAM CAPSULE ENDOSCOPE SYSTEM
GIVEN PILLCAM PLATFORM WITH RAPID 6.5 / GIVEN PILLCAM PLATFORM WITH PILLCAM ESO 3 CAPSULES
GIVEN PILLCAM PLATFORM WITH PILLCAM SB CAPSULES
GIVEN PILLCAM PLATFORM WITH PILLCAM SB CAPSULESWITH PILLCAM R SENSORBELT
PILLCAM EXPRESS VIDEO CAPSULES DELIVERY DEVICE
MODIFICATION TO OLYMPUS CAPSULE ENDOSCOPE SYSTEM
PILLCAM PLATFORM WITH PILLCAM SB CAPSULES WITH PILLCAM SENSORBELT
OLYMPUS CAPSULE ENDOSCOPE SYSTEM
MODIFICATON TO: GIVEN DIAGNOSTIC IMAGING SYSTEM
MODIFICATION TO GIVEN DIAGNOSTIC SYSTEM
GIVEN DIAGNOSTIC SYSTEM
CAPSULE DELIVERY DEVICE, 160CM, MODEL 711143; CAPSULE DELIVERY DEVICE, 210CM, MODEL 711144
MODIFICATION TO GIVEN DIAGNOSTIC SYSTEM
GIVEN DIAGNOSTIC SYSTEM
GIVEN DIAGNOSTIC SYSTEM
MODIFICATION TO GIVEN DIAGNOSTIC SYSTEM
GIVEN DIAGNOSTICS SYSTEM
GIVEN DIAGNOSTIC SYSTEM
GIVEN DIAGNOSTIC IMAGING SYSTEM

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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