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SPECTACLE FRAMES+ SUNGLASSSES(NON PRESC.)

K914954 Class I Traditional
Decision Date
1992-02-27
Sponsor / Applicant
Jsu Corp.

Technical Specification

510(k) Submission ID K914954
Product Code HQZ
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.5842
Decision Date 1992-02-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SPECTACLE FRAMES+ SUNGLASSSES(NON PRESC.) received FDA 510(k) clearance under submission number K914954, sponsored by Jsu Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 1992-02-27.

Classification & Regulation

This clearance is catalogued under FDA product code HQZ and 21 CFR 886.5842, within the Ophthalmic review panel as a Class I device.