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Recognized a 510(k)/PMA number — showing its clearance record and devices.

Clearance record K220108

SDC4K Information Management System with Device and Voice Control Package · Stryker Endoscopy · decided 2022-02-09 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
SDC4K0240300100STRYKER CORPORATIONGCJ HRX07613327562750