Cleared Traditional

K052891 - HORIZON EPIKERATOME DISPOSABLE MICROKERATOME SYSTEM

K052891 is an FDA 510(k) clearance for HORIZON EPIKERATOME DISPOSABLE MICROKER..., manufactured by Hawken Industries. The device is a Class 1 Ophthalmic device with product code HNO cleared through the Traditional 510(k) pathway after a 161-day FDA review.

K052891 · Hawken Industries · Ophthalmic device
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Mar 2006
Decision
161d
Days
Class 1
Risk

K052891 is an FDA 510(k) clearance for the HORIZON EPIKERATOME DISPOSABLE MICROKERATOME SYSTEM. Classified as Keratome, Ac-powered (product code HNO), Class I - General Controls.

Submitted by Hawken Industries (Hasbrouck Heights, US). The FDA issued a Cleared decision on March 23, 2006 after a review of 161 days - an extended review cycle.

This device falls under the Ophthalmic FDA review panel, regulated under 21 CFR 886.4370 - 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 Hawken Industries devices

FDA 510(k) Submission Details - K052891

510(k) Number K052891 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 13, 2005
Decision Date March 23, 2006
Days to Decision 161 days
Submission Type Traditional
Review Panel Ophthalmic (OP)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
51d slower than avg
Panel avg: 110d · This submission: 161d
Pathway characteristics
Predicate-based equivalence.

HNO Device Classification - Class 1, General Controls

Product Code HNO Keratome, Ac-powered
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 886.4370
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 - HNO Keratome, Ac-powered

All 43
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