Clearance Summary
EndoScreener received FDA 510(k) clearance under submission number K211326, sponsored by Chengdu Wision Medical Device Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2021-11-19.
- Submission: K211326
- Applicant / Sponsor: Chengdu Wision Medical Device Co., Ltd.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.1520
- Decision date: 2021-11-19
Classification & Regulation
This clearance is catalogued under FDA product code QNP and 21 CFR 876.1520, within the Gastroenterology, Urology review panel as a Class II device.