ZenPro 40

ZenPro 40 is the device name listed in this FDA 510(k) record. The listed applicant is BLUECORE COMPANY Co., Ltd.. It received FDA 510(k) clearance on 2023-08-10 under 510(k) number K230268. The device is classified under product code GEX. It was reviewed by the SU advisory panel. Product code GEX falls under the category of Gastroenterology, which includes gastrointestinal diagnostic and therapeutic devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.