Clearance Summary
MENICON PROGENT REMOVER FOR RIGID GAS PERMEABLE CONTACT LENSES received FDA 510(k) clearance under submission number K020930, sponsored by Menicon Co, 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 2002-05-02.
- Submission: K020930
- Applicant / Sponsor: Menicon Co, Ltd.
- Clearance pathway: Traditional
- Review panel: Ophthalmic
- Device class: Class II
- Regulation citation: 21 CFR 886.5918
- Decision date: 2002-05-02
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.