meddevicedb.com FDA Device Reference

RIGID GAS PERMEABLE CONTACT LENS

K013762 Class II Traditional
Decision Date
2002-04-03
Sponsor / Applicant
Bausch & Lomb, Incorporated

Technical Specification

510(k) Submission ID K013762
Product Code HQD
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.5916
Decision Date 2002-04-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RIGID GAS PERMEABLE CONTACT LENS received FDA 510(k) clearance under submission number K013762, sponsored by Bausch & Lomb, Incorporated. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 2002-04-03.

Classification & Regulation

This clearance is catalogued under FDA product code HQD and 21 CFR 886.5916, within the Ophthalmic review panel as a Class II device.