Clearance Summary
BARNES-HIND SPECTACLE LENS CLEANER received FDA 510(k) clearance under submission number K811554, sponsored by Barnes-Hind, 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 1981-07-02.
- Submission: K811554
- Applicant / Sponsor: Barnes-Hind, Inc.
- Clearance pathway: Traditional
- Review panel: Ophthalmic
- Device class: Class I
- Regulation citation: 21 CFR 886.5844
- Decision date: 1981-07-02
Classification & Regulation
This clearance is catalogued under FDA product code HQG and 21 CFR 886.5844, within the Ophthalmic review panel as a Class I device.