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CR-39 PLASTIC LENSES FOR EYEGLASSES

K882308 Class I Traditional
Decision Date
1988-07-22
Sponsor / Applicant
Automated Lens System

Technical Specification

510(k) Submission ID K882308
Product Code HQG
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.5844
Decision Date 1988-07-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CR-39 PLASTIC LENSES FOR EYEGLASSES received FDA 510(k) clearance under submission number K882308, sponsored by Automated Lens System. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 1988-07-22.

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.