meddevicedb.com FDA Device Reference

POSTOPERATIVE UV GLASSES (PLANO/APHAKIC)

K802651 Class I Traditional
Decision Date
1980-12-17
Sponsor / Applicant
Chiron Vision Corp.

Technical Specification

510(k) Submission ID K802651
Product Code HQG
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.5844
Decision Date 1980-12-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

POSTOPERATIVE UV GLASSES (PLANO/APHAKIC) received FDA 510(k) clearance under submission number K802651, sponsored by Chiron Vision 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 1980-12-17.

Classification & Regulation

This clearance is catalogued under FDA product code HQG and 21 CFR 886.5844, within the Ophthalmic review panel as a Class I device.