Clearance Summary
PENTEX EC-3890LI received FDA 510(k) clearance under submission number K093037, sponsored by Pentax Medical Company. 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 2009-12-28.
- Submission: K093037
- Applicant / Sponsor: Pentax Medical Company
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.1500
- Decision date: 2009-12-28
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.