meddevicedb.com FDA Device Reference

SPECTACLE FRAMES AND SUNGLASSES

K933189 Class I Traditional
Decision Date
1994-01-25
Sponsor / Applicant
Eastern Breeze Intl. Co.

Technical Specification

510(k) Submission ID K933189
Product Code HQY
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.5850
Decision Date 1994-01-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SPECTACLE FRAMES AND SUNGLASSES received FDA 510(k) clearance under submission number K933189, sponsored by Eastern Breeze Intl. Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 1994-01-25.

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.