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: ODA FDA class 2

Endoscopic Central Control Unit

Gastroenterology, Urology

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The Endoscopic Central Control Unit (product code ODA) is a gastroenterology and urology device used to control endoscopic and ancillary surgical equipment from one central location, via remote control, touch screen, or voice command, streamlining operation in the endoscopy suite or operating room. Integration of control functions improves workflow and reduces the need for manual equipment adjustments during procedures. 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

18 matches
K Number
Device Name
KARL STORZ OR1™ SCB CONTROL (WU300)
Smith+Nephew INTELLIO Tablet
Tablet Application
INTELLIO Tablet Application
IDSS ForceTriad Control Module
core nova Complete Operating Room Endoscopy
KARL STORZ SCB / COVIDIEN FORCETRIAD INTERFACE MODULE
SYSTEMS INTEGRATION
SYSTEMS INTEGRATION MODEL: ENDOALPHA
KARL STORZ VOICE1 SCB R-UI SPEECH CONTROL APPLICATION
KARL STORZ SCB/CONMED ESU INTERFACE MODULE, MODEL 20091522
KARL STORZ SCB INTERFACE CONTROL, MODEL 20090120
MODIFICATION TO OLYMPUS INTEGRATED ENDOSURGERY SYSTEM ENDOALPHA (CONTROL UNIT FOR ENDOSURGERY UCES-2) SOFTWARE VERSION 3
SCB/VALLEYLAB FORCE FX INTERFACE UNIT
RIWO NET OPERATING OPERATING CONTROL SYSTEM, MODEL #5590
MODIFICATION TO OLYMPUS INTEGRATED ENDOSURGERY SYSTEM ENDOALPHA
SIEMENS INTEGRATED OPERATING SYSTEM (SIOS)
OLYMPUS INTEGRATED ENDOSURGERY SYSTEM ENDOALPHA

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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