meddevicedb.com FDA Device Reference

SPECTACLE, FRAME AND SUNGLASSES

K881278 Class I Traditional
Decision Date
1988-05-25
Sponsor / Applicant
Nouvelle Ligne Paris

Technical Specification

510(k) Submission ID K881278
Product Code HQY
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.5850
Decision Date 1988-05-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SPECTACLE, FRAME AND SUNGLASSES received FDA 510(k) clearance under submission number K881278, sponsored by Nouvelle Ligne Paris. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 1988-05-25.

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.