Clearance Summary
NIDEK KM-800 AUTO KERATOMETER received FDA 510(k) clearance under submission number K861063, sponsored by Nidek, 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 1986-04-04.
- Submission: K861063
- Applicant / Sponsor: Nidek, Inc.
- Clearance pathway: Traditional
- Review panel: Ophthalmic
- Device class: Class I
- Regulation citation: 21 CFR 886.1350
- Decision date: 1986-04-04
Classification & Regulation
This clearance is catalogued under FDA product code HLQ and 21 CFR 886.1350, within the Ophthalmic review panel as a Class I device.