meddevicedb.com FDA Device Reference

SUN/SPORTGLASSES

K920211 Class I Traditional
Decision Date
1992-05-01
Sponsor / Applicant
Bacou USA, Inc. and Uvex Safety, Inc.

Technical Specification

510(k) Submission ID K920211
Product Code HQY
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.5850
Decision Date 1992-05-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SUN/SPORTGLASSES received FDA 510(k) clearance under submission number K920211, sponsored by Bacou USA, Inc. and Uvex Safety, 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 1992-05-01.

Classification & Regulation

This clearance is catalogued under FDA product code HQY and 21 CFR 886.5850, within the Ophthalmic review panel as a Class I device.