meddevicedb.com FDA Device Reference

ARCTIC PREMIER SERIES

K944700 Class I Traditional
Decision Date
1994-12-22
Sponsor / Applicant
Sungold Eyewear, Inc.

Technical Specification

510(k) Submission ID K944700
Product Code HOY
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.4750
Decision Date 1994-12-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ARCTIC PREMIER SERIES received FDA 510(k) clearance under submission number K944700, sponsored by Sungold Eyewear, 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 1994-12-22.

Classification & Regulation

This clearance is catalogued under FDA product code HOY and 21 CFR 886.4750, within the Ophthalmic review panel as a Class I device.