meddevicedb.com FDA Device Reference

SUNGLASSES

K931525 Class I Traditional
Decision Date
1993-08-09
Sponsor / Applicant
Premiums Promotions & Imports, Inc.

Technical Specification

510(k) Submission ID K931525
Product Code HQY
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.5850
Decision Date 1993-08-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SUNGLASSES received FDA 510(k) clearance under submission number K931525, sponsored by Premiums Promotions & Imports, 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 1993-08-09.

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.