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: FWF FDA class 1

Camera, Television, Endoscopic, Without Audio

General, Plastic Surgery

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An endoscopic television camera without audio is a video imaging device integrated with or attached to an endoscope to capture real-time images of internal structures during minimally invasive surgical procedures, without audio. It is classified as FDA Class 1 (lowest risk), subject to general controls only, and does not require premarket notification. The product code is FWF, regulated under 21 CFR 878.4160, within the General, Plastic Surgery medical specialty. No special flags apply to this device.

510(k) Clearances

23 matches
K Number
Device Name
FLEXISCOPE, MODELS 50MH AND 50 MHC
KARL STORZ DIRECT COUPLED INTERFACE (DCI 5) CAMERA SYSTEM
EC-1000-7 DIGITAL ENDOSCOPY VIDEO CAMERA, MODELS EC 1000-7P (PAL) & EC 1000-7N (NTSC)
ENDOCAM CAMERA SYSTEMS 5502/5507 WITH CR CAMERA HEADS AND ACCESSORIES
VES 3001-M COMPLETE VIDEO ENDOSCOPIC SYSTEM
VES 1501-M
ANGIOLAZ VES-1CAM
ISOLATED CAMERA HEAD
FUJINON VIDEO LAPAROSCOPE, MODIFIED
SURGICAL VIDEO CAMERA AND ACCESSORIES
ENDOSCOPIC VIDEO CAMERA
COAST VIDEO ENDOSCOPIC IMAGING SYSTEM
VIDEO CAMERA W/ ELECTRONIC SHUTTER MODEL VCE-10
INTEGRATED VISUALIZATION SYSTEM
3DSCOPE
IMAGYN MEDICAL VIDEOSCOPY SYST W/IRRIG PUMP/ACCESS
HC-SERIES MEDICAL CAMERA/LIGHT SOURCE AND ACCESSOR
THE KARL STORZ MINI 9000 SOLID STATE CCD VIDEO CAM
RGB CAMERA SYSTEM
MEDICAM S-4 SURGICAL CAMERA
MODEL MC-1 SURGICAL VIDEO CAMERA
VIDEO CAMERA SYSTEM
ARTHROSCAN VIDEO 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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