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OCS 100 (OCULAR COMPARATOR SYSTEM)

K874220 Class II Traditional
Decision Date
1987-12-23
Sponsor / Applicant
Ocular Instruments, Inc.

Technical Specification

510(k) Submission ID K874220
Product Code HJO
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.1850
Decision Date 1987-12-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OCS 100 (OCULAR COMPARATOR SYSTEM) received FDA 510(k) clearance under submission number K874220, sponsored by Ocular Instruments, 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 1987-12-23.

Classification & Regulation

This clearance is catalogued under FDA product code HJO and 21 CFR 886.1850, within the Ophthalmic review panel as a Class II device.