Clearance Summary
CLEAR LENS ENDOSCOPIC FOG REDUCTION DEVICE received FDA 510(k) clearance under submission number K942576, sponsored by White Knight Healthcare. 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 1994-07-05.
- Submission: K942576
- Applicant / Sponsor: White Knight Healthcare
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.1500
- Decision date: 1994-07-05
Classification & Regulation
This clearance is catalogued under FDA product code OCT and 21 CFR 876.1500, within the Gastroenterology, Urology review panel as a Class II device.