meddevicedb.com FDA Device Reference

SPECTACLE FRAMES

K932439 Class I Traditional
Decision Date
1994-01-03
Sponsor / Applicant
Styl-Rite Optics, Inc.

Technical Specification

510(k) Submission ID K932439
Product Code HQZ
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.5842
Decision Date 1994-01-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SPECTACLE FRAMES received FDA 510(k) clearance under submission number K932439, sponsored by Styl-Rite Optics, 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 1994-01-03.

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.