meddevicedb.com FDA Device Reference

MULTIPLE SPECTACLE FRAMES

K883100 Class I Traditional
Decision Date
1988-08-25
Sponsor / Applicant
Metal Optics U.S.A., Inc.

Technical Specification

510(k) Submission ID K883100
Product Code HQZ
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.5842
Decision Date 1988-08-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MULTIPLE SPECTACLE FRAMES received FDA 510(k) clearance under submission number K883100, sponsored by Metal Optics U.S.A., 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 1988-08-25.

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.