Clearance Summary
Kowa SL-19 received FDA 510(k) clearance under submission number K222372, sponsored by Kowa Company , 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 2022-11-21.
- Submission: K222372
- Applicant / Sponsor: Kowa Company , Ltd.
- Clearance pathway: Traditional
- Review panel: Ophthalmic
- Device class: Class II
- Regulation citation: 21 CFR 886.1850
- Decision date: 2022-11-21
Classification & Regulation
This clearance is catalogued under FDA product code HJO and 21 CFR 886.1850, within the Ophthalmic review panel as a Class II device.