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EYEGLASS SPECTACLE FRAMES VARIOUS COLLECTIONS

K941052 Class I Traditional
Decision Date
1994-04-12
Sponsor / Applicant
Atlantic Optical Co., Inc.

Technical Specification

510(k) Submission ID K941052
Product Code HQZ
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.5842
Decision Date 1994-04-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EYEGLASS SPECTACLE FRAMES VARIOUS COLLECTIONS received FDA 510(k) clearance under submission number K941052, sponsored by Atlantic Optical Co., 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 1994-04-12.

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.