Clearance Summary
NIL received FDA 510(k) clearance under submission number K944641, sponsored by Max-Vision (H.K.)Limited. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 1994-11-14.
- Submission: K944641
- Applicant / Sponsor: Max-Vision (H.K.)Limited
- Clearance pathway: Traditional
- Review panel: Ophthalmic
- Device class: Class I
- Regulation citation: 21 CFR 886.5842
- Decision date: 1994-11-14
Classification & Regulation
This clearance is catalogued under FDA product code HQZ and 21 CFR 886.5842, within the Ophthalmic review panel as a Class I device.