Clearance Summary
FRESENIUS ULTRAFLUX HEMODIALYZER received FDA 510(k) clearance under submission number K031378, sponsored by Fresenius Medical Care North America. 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 2003-05-30.
- Submission: K031378
- Applicant / Sponsor: Fresenius Medical Care North America
- Clearance pathway: Special
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.5860
- Decision date: 2003-05-30
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.