meddevicedb.com FDA Device Reference

SPECTACLE FRAMES

K936146 Class I Traditional
Decision Date
1994-02-22
Sponsor / Applicant
Franel Optical

Technical Specification

510(k) Submission ID K936146
Product Code HQY
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.5850
Decision Date 1994-02-22
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 K936146, sponsored by Franel Optical. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 1994-02-22.

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.