Clearance Summary
SPECTACLE FRAMES received FDA 510(k) clearance under submission number K934301, sponsored by Gernot Lindner, Lunor-Vertrieb. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 1993-12-08.
- Submission: K934301
- Applicant / Sponsor: Gernot Lindner, Lunor-Vertrieb
- Clearance pathway: Traditional
- Review panel: Ophthalmic
- Device class: Class I
- Regulation citation: 21 CFR 886.5842
- Decision date: 1993-12-08
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.