Clearance Summary
KOWA HAND-HELD APPLANATION TONOMETER HA-1 received FDA 510(k) clearance under submission number K960924, sponsored by Kowa Optimed, 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 1996-06-04.
- Submission: K960924
- Applicant / Sponsor: Kowa Optimed, Inc.
- Clearance pathway: Traditional
- Review panel: Ophthalmic
- Device class: Class II
- Regulation citation: 21 CFR 886.1930
- Decision date: 1996-06-04
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.