Clearance Summary
WAK WEARABLE ARTIFICIAL KIDNEY received FDA 510(k) clearance under submission number K830291, sponsored by Wak-Utah. 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 1983-03-29.
- Submission: K830291
- Applicant / Sponsor: Wak-Utah
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.5820
- Decision date: 1983-03-29
Classification & Regulation
This clearance is catalogued under FDA product code KOC and 21 CFR 876.5820, within the Gastroenterology, Urology review panel as a Class II device.