Clearance Summary
PRISMA HF 1000 SET, PRISMA HF 1000 PRE-SET received FDA 510(k) clearance under submission number K011221, sponsored by Gambro Renal Products. 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 2001-10-31.
- Submission: K011221
- Applicant / Sponsor: Gambro Renal Products
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.5860
- Decision date: 2001-10-31
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.