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EUCLID SYSTEMS CORNEAL TOPOGRAPHER MODEL ET800

K964702 Class I Traditional
Decision Date
1997-05-20
Sponsor / Applicant
Euclid Systems Corp.

Technical Specification

510(k) Submission ID K964702
Product Code MMQ
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.1350
Decision Date 1997-05-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EUCLID SYSTEMS CORNEAL TOPOGRAPHER MODEL ET800 received FDA 510(k) clearance under submission number K964702, sponsored by Euclid Systems Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 1997-05-20.

Classification & Regulation

This clearance is catalogued under FDA product code MMQ and 21 CFR 886.1350, within the Ophthalmic review panel as a Class I device.