Clearance Summary
VISUAL ENDOSCOPIC NON-ALCOHOL ULTRACELL SPONGE (VENUS) received FDA 510(k) clearance under submission number K973558, sponsored by Ultracell Medical Technologies, 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 1997-11-24.
- Submission: K973558
- Applicant / Sponsor: Ultracell Medical Technologies, Inc.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.1500
- Decision date: 1997-11-24
Classification & Regulation
This clearance is catalogued under FDA product code FEB and 21 CFR 876.1500, within the Gastroenterology, Urology review panel as a Class II device.