Clearance Summary
CORDIS DOW C-DAK 1.8MRC ARTIFIC-KIDNEY received FDA 510(k) clearance under submission number K802894, 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 1981-02-19.
- Submission: K802894
- Applicant / Sponsor: Cordis Corp.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.5820
- Decision date: 1981-02-19
Classification & Regulation
This clearance is catalogued under FDA product code FJI and 21 CFR 876.5820, within the Gastroenterology, Urology review panel as a Class II device.