Clearance Summary
Matrix Pre-Treatment Controller received FDA 510(k) clearance under submission number K161844, sponsored by Better Water, LLC. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2016-12-13.
- Submission: K161844
- Applicant / Sponsor: Better Water, LLC
- Clearance pathway: Abbreviated
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.5665
- Decision date: 2016-12-13
Classification & Regulation
This clearance is catalogued under FDA product code FIP and 21 CFR 876.5665, within the Gastroenterology, Urology review panel as a Class II device.