Clearance Summary
SPECTACLE, MAGNIFYING received FDA 510(k) clearance under submission number K873967, sponsored by Swank Plus , 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 1988-02-26.
- Submission: K873967
- Applicant / Sponsor: Swank Plus , Ltd.
- Clearance pathway: Traditional
- Review panel: Ophthalmic
- Device class: Class I
- Regulation citation: 21 CFR 886.5910
- Decision date: 1988-02-26
Classification & Regulation
This clearance is catalogued under FDA product code HOT and 21 CFR 886.5910, within the Ophthalmic review panel as a Class I device.