Monarch Iol Delivery System

FDA 510(k) K970033 · Alcon Laboratories

Substantially Equivalent

510(k) numberK970033

Submission

Device name
Monarch Iol Delivery System
Applicant
Alcon Laboratories
Fort Worth, TX, US
Received
January 3, 1997
Decision date
April 23, 1997
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
KYB – Lens, Guide, Intraocular
Device class
Class I (low risk)
Regulation
21 CFR 886.4300
Specialty
Ophthalmic

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K072985Duckworth & Kent Ltd Injector, Model: DK7797-2KYB · Traditional Duckworth & Kent, Ltd.06/20/2008SE
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K022723Mastel 1 Folder Implantation SystemKYB · Traditional Mastel Precision, Inc.12/26/2002SE
K001157Monarch II Iol Delivery SystemKYB · Traditional Alcon Research, Ltd.06/27/2000SE
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Questions and answers

When was Monarch Iol Delivery System cleared by the FDA?

Monarch Iol Delivery System (K970033) received a 510(k) decision of Substantially Equivalent on April 23, 1997, 110 days after the submission was received.

What is the product code of K970033?

The FDA product code is KYB – Lens, Guide, Intraocular, a Class I (low risk) device regulated under 21 CFR 886.4300.