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: OCV FDA class 2

Endoscope Holder

Gastroenterology, Urology

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The Endoscope Holder (product code OCV) is a gastroenterology and urology accessory used to hold an endoscope in a desired position during diagnostic or therapeutic procedures, freeing the clinician's hands and stabilizing the instrument. Stable endoscope positioning is important for precision during complex endoscopic interventions. This device is FDA Class 2 under regulation 876.1500 in the Gastroenterology, Urology specialty, requiring 510(k) clearance and compliance with general and special controls. It carries no implant or life-sustaining flags.

510(k) Clearances

10 matches
K Number
Device Name
KARL STORZ Holders
ENDOFIX EXO
WalterLorenz Surgical Assist Arm Scope Holder
ENVIEW (TM)
V. MUELLER CAMERA CONTROLLER WITH STORAGE CART
NEUROVIEW INSTRUMENT HOLDER, MODEL 300-33
KSEA ENDOSCOPE HOLDER
CLARUS MODEL 2127-900 SERIES ENDOSCOPE ADATER (2127-900 SERIES)
SH-1 SURGICAL HOLDER FOR TELESCOPE
UROLOGIC TUBE HOLDER

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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