Clearance Summary
LABORIE FIBREOPTIC LIGHT CABLE received FDA 510(k) clearance under submission number K840605, sponsored by Tridak Division of Indicon, 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 1984-04-13.
- Submission: K840605
- Applicant / Sponsor: Tridak Division of Indicon, Inc.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.1500
- Decision date: 1984-04-13
Classification & Regulation
This clearance is catalogued under FDA product code FFS and 21 CFR 876.1500, within the Gastroenterology, Urology review panel as a Class II device.