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SUNGLASSES (FRAME,CELLULOSE PROPINATE, LENS, ACRYLIC)

K971087 Class I Traditional
Decision Date
1997-06-13
Sponsor / Applicant
W.J. Byrnes & Co. of Los Angeles, Inc.

Technical Specification

510(k) Submission ID K971087
Product Code HQY
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.5850
Decision Date 1997-06-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SUNGLASSES (FRAME,CELLULOSE PROPINATE, LENS, ACRYLIC) received FDA 510(k) clearance under submission number K971087, sponsored by W.J. Byrnes & Co. of Los Angeles, 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 1997-06-13.

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.