Clearance Summary
TUNA SYSTEM, MODELS 8909, 8929, 8930, 8934 received FDA 510(k) clearance under submission number K052413, sponsored by Medtronic Vascular. 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 2005-11-17.
- Submission: K052413
- Applicant / Sponsor: Medtronic Vascular
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.4300
- Decision date: 2005-11-17
Classification & Regulation
This clearance is catalogued under FDA product code KNS and 21 CFR 876.4300, within the Gastroenterology, Urology review panel as a Class II device.