Clearance Summary
GAMBRO PRISMAFLEX AND GAMBRO PRISMAFLEX M60 & M100 SETS received FDA 510(k) clearance under submission number K041005, sponsored by Gambro Renal Products. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2004-10-07.
- Submission: K041005
- Applicant / Sponsor: Gambro Renal Products
- Clearance pathway: Abbreviated
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.5860
- Decision date: 2004-10-07
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.