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: OCT FDA class 2

Anti Fog Solution And Accessories, Endoscopy

Gastroenterology, Urology

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The Anti-Fog Solution and Accessories for Endoscopy (product code OCT) is a gastroenterology and urology accessory used to prevent, reduce, or eliminate condensation (fogging) on endoscopic lenses during procedures, maintaining clear visualization throughout the examination. It may include solution, sprays, or other components applied to endoscope optics. This device is FDA Class 2 under regulation 876.1500 in the Gastroenterology, Urology specialty, requires 510(k) clearance, and is eligible for third-party review. It carries no implant or life-sustaining flags.

510(k) Clearances

27 matches
K Number
Device Name
KnoxFog Anti-fogging Device
GOLFF Sterile Anti-Fog Solution
E-Brik Visualization Assistant
Konix Anti-Fog Solution
AMD Anti-Fog Solution
VitreOx Anti-fog Solution
Medline Anti-Fog Solution
LLICS(TM) LAPARASCOPIC LENS INTERNAL CLEANING SYSTEM
UNIMAX ANTI-FOG SOLUTION
DEFOGGING AND CLEANING SOLUTION- FLO-X
CLEAR-VU SYSTEM, MODELS: CVL-01-1000, CVL-01-1030, CVL-01-1045
XODUS MEDICAL ANTI-FOG SOLUTION
ORS MODEL 6000 ENDOSCOPE HOLDER
CLEAR-IT ANTI-FOG, MODEL PS003
ENDOSCOPIC ANTI FOG DEVICE
DEROYAL INDUSTRIES, INC. DEFOGGER
CLEARFIELD ANTI-FOG STERILE WIPE, PRODUCT NUMBER 300-004
FOG FREE
CLEAR LENS ENDOSCOPIC FOG REDUCTION DEVICE
FOGLESS
EAGLE MEDICAL ANTI-FOG KIT
SURGICOT FOG FREE
FOG CONTROL, LENS FOG REDUCTION DEVICE
U.C.E.Z. LENS CLEANER KIT
DR. FOG
MEDI-KLEER
UCEZ - STERILE LENS FOG REDUCTION DEVICE

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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