Clearance Summary
2008 HEMODIALYSIS SORBENT SYSTEM received FDA 510(k) clearance under submission number K123835, sponsored by Renal Solutions, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2013-02-15.
- Submission: K123835
- Applicant / Sponsor: Renal Solutions, Inc.
- Clearance pathway: Special
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.5600
- Decision date: 2013-02-15
Classification & Regulation
This clearance is catalogued under FDA product code FKT and 21 CFR 876.5600, within the Gastroenterology, Urology review panel as a Class II device.