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STANDARD CONTACT LENS CASE; FLIP N SLIDE CONTACT LENS CASE

K130753 Class II Traditional
Decision Date
2013-06-13
Sponsor / Applicant
Watchdog Group, LC

Technical Specification

510(k) Submission ID K130753
Product Code LRX
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.5928
Decision Date 2013-06-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

STANDARD CONTACT LENS CASE; FLIP N SLIDE CONTACT LENS CASE received FDA 510(k) clearance under submission number K130753, sponsored by Watchdog Group, LC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 2013-06-13.

Classification & Regulation

This clearance is catalogued under FDA product code LRX and 21 CFR 886.5928, within the Ophthalmic review panel as a Class II device.