meddevicedb.com FDA Device Reference

SUNGLASSES (NON-PRESCRIPTION)

K935114 Class I Traditional
Decision Date
1994-02-22
Sponsor / Applicant
Promising Enterprise CO , Ltd.

Technical Specification

510(k) Submission ID K935114
Product Code HQY
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.5850
Decision Date 1994-02-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SUNGLASSES (NON-PRESCRIPTION) received FDA 510(k) clearance under submission number K935114, sponsored by Promising Enterprise 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 1994-02-22.

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.