Clearance Summary
KERATRON CORNEAL TOPOGRAPHER received FDA 510(k) clearance under submission number K944616, sponsored by Alliance Medical Marketinig. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 1994-11-22.
- Submission: K944616
- Applicant / Sponsor: Alliance Medical Marketinig
- Clearance pathway: Traditional
- Review panel: Ophthalmic
- Device class: Class I
- Regulation citation: 21 CFR 886.1350
- Decision date: 1994-11-22
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.