Clearance Summary
C-DAK DUO-FLUX ARTIFICIAL KIDNEY received FDA 510(k) clearance under submission number K801731, sponsored by Cordis 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 1980-08-13.
- Submission: K801731
- Applicant / Sponsor: Cordis Corp.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.5860
- Decision date: 1980-08-13
Classification & Regulation
This clearance is catalogued under FDA product code KDI and 21 CFR 876.5860, within the Gastroenterology, Urology review panel as a Class II device.