Clearance Summary
LUNEAU STERILE TONOMETER SEPARATION PRISMS received FDA 510(k) clearance under submission number K023838, sponsored by Luneau SA. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 2003-02-20.
- Submission: K023838
- Applicant / Sponsor: Luneau SA
- Clearance pathway: Traditional
- Review panel: Ophthalmic
- Device class: Class II
- Regulation citation: 21 CFR 886.1930
- Decision date: 2003-02-20
Classification & Regulation
This clearance is catalogued under FDA product code HKY and 21 CFR 886.1930, within the Ophthalmic review panel as a Class II device.