Clearance Summary
EDWARDS AQUARIUS HEMOFILTRATION SYSTEM, MODEL ABM 01 received FDA 510(k) clearance under submission number K070320, sponsored by Edwards Lifesciences Services GmbH. 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 2007-06-07.
- Submission: K070320
- Applicant / Sponsor: Edwards Lifesciences Services GmbH
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.5860
- Decision date: 2007-06-07
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.