Clearance Summary
OPTI-FREE SUPRACLENS DAILY POTEIN REMOVER / RGP MULTI-PURPOSE DISINFECTING SOLUTION ID 100136 received FDA 510(k) clearance under submission number K001235, sponsored by Alcon Universal, Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 2000-07-03.
- Submission: K001235
- Applicant / Sponsor: Alcon Universal, Ltd.
- Clearance pathway: Traditional
- Review panel: Ophthalmic
- Device class: Class II
- Regulation citation: 21 CFR 886.5918
- Decision date: 2000-07-03
Classification & Regulation
This clearance is catalogued under FDA product code MRC and 21 CFR 886.5918, within the Ophthalmic review panel as a Class II device.