meddevicedb.com FDA Device Reference

EYE SPHERES

K082850 Class II Traditional
Decision Date
2009-02-27
Sponsor / Applicant
Product and Educational Services, LLC

Technical Specification

510(k) Submission ID K082850
Product Code HPZ
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.3320
Decision Date 2009-02-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EYE SPHERES received FDA 510(k) clearance under submission number K082850, sponsored by Product and Educational Services, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 2009-02-27.

Classification & Regulation

This clearance is catalogued under FDA product code HPZ and 21 CFR 886.3320, within the Ophthalmic review panel as a Class II device.