Clearance Summary
GOLDMAN MANUAL TONOMETER received FDA 510(k) clearance under submission number K981432, sponsored by Golden Vision, 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 1999-01-12.
- Submission: K981432
- Applicant / Sponsor: Golden Vision, Inc.
- Clearance pathway: Traditional
- Review panel: Ophthalmic
- Device class: Class II
- Regulation citation: 21 CFR 886.1930
- Decision date: 1999-01-12
Classification & Regulation
This clearance is catalogued under FDA product code HKY and 21 CFR 886.1930, within the Ophthalmic review panel as a Class II device.