Clearance Summary
CANON SURGICAL AUTO KERATOMETER SK-1 received FDA 510(k) clearance under submission number K871936, sponsored by Canon USA, 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 1987-06-19.
- Submission: K871936
- Applicant / Sponsor: Canon USA, Inc.
- Clearance pathway: Traditional
- Review panel: Ophthalmic
- Device class: Class I
- Regulation citation: 21 CFR 886.1350
- Decision date: 1987-06-19
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.