Clearance Summary
K.E.A.T. received FDA 510(k) clearance under submission number K002154, sponsored by Emd Electronic Medical Devices, Corp.. 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 2001-03-22.
- Submission: K002154
- Applicant / Sponsor: Emd Electronic Medical Devices, Corp.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.5320
- Decision date: 2001-03-22
Classification & Regulation
This clearance is catalogued under FDA product code KPI and 21 CFR 876.5320, within the Gastroenterology, Urology review panel as a Class II device.