Clearance Summary
VIASPAN (BELZER UW - CSS) received FDA 510(k) clearance under submission number K944866, sponsored by The Dupont Merck Pharmaceutical Co.. 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 1996-04-22.
- Submission: K944866
- Applicant / Sponsor: The Dupont Merck Pharmaceutical Co.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.5880
- Decision date: 1996-04-22
Classification & Regulation
This clearance is catalogued under FDA product code KDL and 21 CFR 876.5880, within the Gastroenterology, Urology review panel as a Class II device.