Clearance Summary
NAVIAID ICVI DEVICE received FDA 510(k) clearance under submission number K101191, sponsored by Smart Medical Systems , Ltd.. 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 2010-07-27.
- Submission: K101191
- Applicant / Sponsor: Smart Medical Systems , Ltd.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.1500
- Decision date: 2010-07-27
Classification & Regulation
This clearance is catalogued under FDA product code FDF and 21 CFR 876.1500, within the Gastroenterology, Urology review panel as a Class II device.