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SPECTACLES LENS

K860955 Class I Traditional
Decision Date
1986-03-31
Sponsor / Applicant
Roseburg SA

Technical Specification

510(k) Submission ID K860955
Product Code HQG
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.5844
Decision Date 1986-03-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SPECTACLES LENS received FDA 510(k) clearance under submission number K860955, sponsored by Roseburg SA. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 1986-03-31.

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.