Clearance Summary
CONTACLAIR MULTI-PURPOSE CONTACT LENS SOLUTION received FDA 510(k) clearance under submission number K994021, sponsored by Strieter Clinical Research Laboratories, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 2000-02-22.
- Submission: K994021
- Applicant / Sponsor: Strieter Clinical Research Laboratories, Inc.
- Clearance pathway: Traditional
- Review panel: Ophthalmic
- Device class: Class II
- Regulation citation: 21 CFR 886.5928
- Decision date: 2000-02-22
Classification & Regulation
This clearance is catalogued under FDA product code LYL and 21 CFR 886.5928, within the Ophthalmic review panel as a Class II device.