Clearance Summary
MODIFICATION TO CIBA VISION CENTURION SES SPIKERATOME received FDA 510(k) clearance under submission number K032978, sponsored by Ciba Vision Corporation. The device was reviewed via the Special premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 2003-10-20.
- Submission: K032978
- Applicant / Sponsor: Ciba Vision Corporation
- Clearance pathway: Special
- Review panel: Ophthalmic
- Device class: Class I
- Regulation citation: 21 CFR 886.4370
- Decision date: 2003-10-20
Classification & Regulation
This clearance is catalogued under FDA product code HNO and 21 CFR 886.4370, within the Ophthalmic review panel as a Class I device.