meddevicedb.com FDA Device Reference

SPECTACLE FRAMES

K810876 Class I Traditional
Decision Date
1981-09-21
Sponsor / Applicant
Fashionline Corp.

Technical Specification

510(k) Submission ID K810876
Product Code HQZ
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.5842
Decision Date 1981-09-21
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 K810876, sponsored by Fashionline 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 1981-09-21.

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.