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DUCKWORTH & KENT LTD LENS DELIVERY SYSTEM

K024072 Class I Traditional
Decision Date
2003-10-06
Sponsor / Applicant
Duckworth & Kent, Ltd.

Technical Specification

510(k) Submission ID K024072
Product Code MSS
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.4300
Decision Date 2003-10-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DUCKWORTH & KENT LTD LENS DELIVERY SYSTEM received FDA 510(k) clearance under submission number K024072, sponsored by Duckworth & Kent, Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 2003-10-06.

Classification & Regulation

This clearance is catalogued under FDA product code MSS and 21 CFR 886.4300, within the Ophthalmic review panel as a Class I device.