Clearance Summary
MODIFICATION TO: USGI SHAPELOCK ENDOSCOPIC GUIDE received FDA 510(k) clearance under submission number K051919, sponsored by Usgi Medical. The device was reviewed via the Special premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2005-07-26.
- Submission: K051919
- Applicant / Sponsor: Usgi Medical
- Clearance pathway: Special
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.1500
- Decision date: 2005-07-26
Classification & Regulation
This clearance is catalogued under FDA product code FED and 21 CFR 876.1500, within the Gastroenterology, Urology review panel as a Class II device.