Shanghai SeeGen Photoelectric Technology Co., Ltd.
Shanghai SeeGen Photoelectric Technology Co., Ltd. — FDA 510(k) Submissions
Shanghai SeeGen Photoelectric Technology Co., Ltd. has submitted 6 FDA 510(k) premarket notifications since 2022, of which 6 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Choledochoscope And Accessories, Flexible/rigid, Ureteroscope And Accessories, Flexible/rigid, Endoscope Channel Accessory, Endoscopic Video Imaging System/component, Gastroenterology-urology, Colonoscope And Accessories, Flexible/rigid . Use the specialty filter in the sidebar to narrow results.