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: FEM FDA class 1

Accessories, Photographic, For Endoscope (Exclude Light Sources)

Gastroenterology, Urology

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Photographic Accessories for Endoscope (excluding light sources) are ancillary components used to capture still or video images during endoscopic examination of the gastrointestinal and urological systems. These accessories are FDA Class 1 devices, representing the lowest risk tier and subject only to general controls. The product code is FEM, regulated under 21 CFR 876.1500, within the Gastroenterology, Urology specialty.

510(k) Clearances

4 matches
K Number
Device Name
CAMERA COVER WITH TEAR TIP
PHOTOGRAPHIC EQUIPMENT
POLAROID INSTANT ENDOCAMERA
POLAROID LAND CAMERA FOR ENDOSCOPY

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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