Clearance Summary
OLYMPUS INTEGRATED ENDOSURGERY SYSTEM ENDOALPHA received FDA 510(k) clearance under submission number K981993, sponsored by The Olympus Optical Co.. 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 1998-08-21.
- Submission: K981993
- Applicant / Sponsor: The Olympus Optical Co.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.1500
- Decision date: 1998-08-21
Classification & Regulation
This clearance is catalogued under FDA product code ODA and 21 CFR 876.1500, within the Gastroenterology, Urology review panel as a Class II device.