meddevicedb.com FDA Device Reference

SUNGLASSES/OPTICAL FRAMES

K854264 Class I Traditional
Decision Date
1985-11-12
Sponsor / Applicant
Wha Chun Industries, Co., Ltd.

Technical Specification

510(k) Submission ID K854264
Product Code HQY
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.5850
Decision Date 1985-11-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SUNGLASSES/OPTICAL FRAMES received FDA 510(k) clearance under submission number K854264, sponsored by Wha Chun Industries, Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 1985-11-12.

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.