Clearance Summary
VESSEL DILATORS received FDA 510(k) clearance under submission number K910502, sponsored by Akcess Medical Products, 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 1991-04-29.
- Submission: K910502
- Applicant / Sponsor: Akcess Medical Products, Inc.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.5540
- Decision date: 1991-04-29
Classification & Regulation
This clearance is catalogued under FDA product code FKA and 21 CFR 876.5540, within the Gastroenterology, Urology review panel as a Class II device.