meddevicedb.com FDA Device Reference

LID CHAIN EYELID WEIGHTS

K021750 Class II Traditional
Decision Date
2003-01-27
Sponsor / Applicant
Jedmed Instrument Co.

Technical Specification

510(k) Submission ID K021750
Product Code MML
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.5700
Decision Date 2003-01-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LID CHAIN EYELID WEIGHTS received FDA 510(k) clearance under submission number K021750, sponsored by Jedmed Instrument Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 2003-01-27.

Classification & Regulation

This clearance is catalogued under FDA product code MML and 21 CFR 886.5700, within the Ophthalmic review panel as a Class II device.