meddevicedb.com FDA Device Reference

DISCOVERY SYSTEM

K133062 Class II Traditional
Decision Date
2014-06-20
Sponsor / Applicant
Innovative Visual Systems

Technical Specification

510(k) Submission ID K133062
Product Code HJO
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.1850
Decision Date 2014-06-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DISCOVERY SYSTEM received FDA 510(k) clearance under submission number K133062, sponsored by Innovative Visual Systems. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 2014-06-20.

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.