Clearance Summary
ENDOLED received FDA 510(k) clearance under submission number K133311, sponsored by Olympus Winter & Ibe GmbH. 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 2014-07-30.
- Submission: K133311
- Applicant / Sponsor: Olympus Winter & Ibe GmbH
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.1500
- Decision date: 2014-07-30
Classification & Regulation
This clearance is catalogued under FDA product code NTN and 21 CFR 876.1500, within the Gastroenterology, Urology review panel as a Class II device.