Clearance Summary
EndoClot received FDA 510(k) clearance under submission number K191254, sponsored by Endoclot Plus 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 2020-01-30.
- Submission: K191254
- Applicant / Sponsor: Endoclot Plus Co., Ltd.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.1500
- Decision date: 2020-01-30
Classification & Regulation
This clearance is catalogued under FDA product code PLL and 21 CFR 876.1500, within the Gastroenterology, Urology review panel as a Class II device.