Cleared Traditional

K041110 - MB 105 MILLENNIUM BLADES

K041110 is an FDA 510(k) clearance for MB 105 MILLENNIUM BLADES, manufactured by Millennium Biomedical, Inc.. The device is a Class 1 Ophthalmic device with product code HNO cleared through the Traditional 510(k) pathway after a 168-day FDA review.

K041110 · Millennium Biomedical, Inc. · Ophthalmic device
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Oct 2004
Decision
168d
Days
Class 1
Risk

K041110 is an FDA 510(k) clearance for the MB 105 MILLENNIUM BLADES. Classified as Keratome, Ac-powered (product code HNO), Class I - General Controls.

Submitted by Millennium Biomedical, Inc. (Pomona, US). The FDA issued a Cleared decision on October 13, 2004 after a review of 168 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 Millennium Biomedical, Inc. devices

FDA 510(k) Submission Details - K041110

510(k) Number K041110 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 28, 2004
Decision Date October 13, 2004
Days to Decision 168 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
58d slower than avg
Panel avg: 110d · This submission: 168d
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 50
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