Clearance Summary
RM3 RENAL PRESERVATION SYSTEM received FDA 510(k) clearance under submission number K053169, sponsored by Waters Instruments, 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 2006-01-17.
- Submission: K053169
- Applicant / Sponsor: Waters Instruments, Inc.
- Clearance pathway: Special
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.5880
- Decision date: 2006-01-17
Classification & Regulation
This clearance is catalogued under FDA product code KDK and 21 CFR 876.5880, within the Gastroenterology, Urology review panel as a Class II device.