Clearance Summary
AMICON DIAFILTER 40. HEMOFILTER received FDA 510(k) clearance under submission number K840449, sponsored by Medical Device Consultants, Inc.. 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 1984-03-23.
- Submission: K840449
- Applicant / Sponsor: Medical Device Consultants, Inc.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.5860
- Decision date: 1984-03-23
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.