Clearance Summary
SPECTACLE FRAMES received FDA 510(k) clearance under submission number K920123, sponsored by Po-Le Optiks. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 1992-03-06.
- Submission: K920123
- Applicant / Sponsor: Po-Le Optiks
- Clearance pathway: Traditional
- Review panel: Ophthalmic
- Device class: Class I
- Regulation citation: 21 CFR 886.5842
- Decision date: 1992-03-06
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.