Clearance Summary
VAN ANDLE DILATION, EMERALD GUIDEWIRE, MODEL VAD6, 502-726 received FDA 510(k) clearance under submission number K002650, sponsored by Bentec Medical, 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 2001-02-16.
- Submission: K002650
- Applicant / Sponsor: Bentec Medical, Inc.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.5010
- Decision date: 2001-02-16
Classification & Regulation
This clearance is catalogued under FDA product code FGE and 21 CFR 876.5010, within the Gastroenterology, Urology review panel as a Class II device.