Clearance Summary
SCLERAL SHELL received FDA 510(k) clearance under submission number K970327, sponsored by Southwest Artificial Eyes, 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 1997-07-07.
- Submission: K970327
- Applicant / Sponsor: Southwest Artificial Eyes, Inc.
- Clearance pathway: Traditional
- Review panel: Ophthalmic
- Device class: Class II
- Regulation citation: 21 CFR 886.3800
- Decision date: 1997-07-07
Classification & Regulation
This clearance is catalogued under FDA product code HQT and 21 CFR 886.3800, within the Ophthalmic review panel as a Class II device.