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STAURENGHI WIDE FIELD SCANNING LASER LENS

K014170 Class II Traditional
Decision Date
2002-03-04
Sponsor / Applicant
Ocular Instruments, Inc.

Technical Specification

510(k) Submission ID K014170
Product Code HJK
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.1385
Decision Date 2002-03-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

STAURENGHI WIDE FIELD SCANNING LASER LENS received FDA 510(k) clearance under submission number K014170, 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 2002-03-04.

Classification & Regulation

This clearance is catalogued under FDA product code HJK and 21 CFR 886.1385, within the Ophthalmic review panel as a Class II device.