Cleared Traditional

K970033 - MONARCH IOL DELIVERY SYSTEM

K970033 is the FDA 510(k) clearance for MONARCH IOL DELIVERY SYSTEM by Alcon Laboratories. It is a Class 1 Ophthalmic device (product code KYB) cleared through the Traditional 510(k) pathway after a 110-day FDA review.

K970033 · Alcon Laboratories · Ophthalmic device
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Apr 1997
Decision
110d
Days
Class 1
Risk

K970033 is an FDA 510(k) clearance for the MONARCH IOL DELIVERY SYSTEM. Classified as Lens, Guide, Intraocular (product code KYB), Class I - General Controls.

Submitted by Alcon Laboratories (Fort Worth, US). The FDA issued a Cleared decision on April 23, 1997 after a review of 110 days - within the typical 510(k) review window.

This device falls under the Ophthalmic FDA review panel, regulated under 21 CFR 886.4300 - the FDA ophthalmic device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Ophthalmic review framework, consistent with the majority of Class II 510(k) submissions.

View all Alcon Laboratories devices

Submission Details

510(k) Number K970033 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 03, 1997
Decision Date April 23, 1997
Days to Decision 110 days
Submission Type Traditional
Review Panel Ophthalmic (OP)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
At panel average
Panel avg: 110d · This submission: 110d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code KYB Lens, Guide, Intraocular
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 886.4300
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - KYB Lens, Guide, Intraocular

All 7
Devices cleared under the same product code (KYB) and FDA review panel - the closest regulatory comparables to K970033.
AKREOS SINGLE USE INSERTION DEVICE, MODEL AI-28
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MONARCH IOL DELIVERY SYSTEM
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K965185 · Alcon Laboratories · Mar 1997
KRATZ NOVA-SERT
K871440 · CooperVision, Inc. · May 1987
KRATZ NOVA-SERT. SOFT INTRAOCULAR LENS INJECTOR
K870265 · CooperVision, Inc. · Feb 1987
SURFACE REPLACEMENT HIP PROSTHESIS
K811718 · Biomet, Inc. · Sep 1981