meddevicedb.com FDA Device Reference

ACTION MEDTEK/DENTEK EYEGLASSES

K925564 Class I Traditional
Decision Date
1993-10-07
Sponsor / Applicant
Action Eyewear Corp.

Technical Specification

510(k) Submission ID K925564
Product Code HOY
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.4750
Decision Date 1993-10-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ACTION MEDTEK/DENTEK EYEGLASSES received FDA 510(k) clearance under submission number K925564, sponsored by Action Eyewear 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 1993-10-07.

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.