Cleared Traditional

K903558 - LASER CANE

K903558 is an FDA 510(k) clearance for LASER CANE, manufactured by Nurion Industries. The device is a Class 1 Ophthalmic device with product code HPG cleared through the Traditional 510(k) pathway after a 50-day FDA review.

K903558 · Nurion Industries · Ophthalmic device
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Sep 1990
Decision
50d
Days
Class 1
Risk

K903558 is an FDA 510(k) clearance for the LASER CANE. Classified as Aid, Vision, Electronic, Battery-powered (product code HPG), Class I - General Controls.

Submitted by Nurion Industries (Paoli, US). The FDA issued a Cleared decision on September 27, 1990 after a review of 50 days - a notably fast clearance cycle.

This device falls under the Ophthalmic FDA review panel, regulated under 21 CFR 886.5900 - 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: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Nurion Industries devices

FDA 510(k) Submission Details - K903558

510(k) Number K903558 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 08, 1990
Decision Date September 27, 1990
Days to Decision 50 days
Submission Type Traditional
Review Panel Ophthalmic (OP)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
60d faster than avg
Panel avg: 110d · This submission: 50d
Pathway characteristics
Predicate-based equivalence.

HPG Device Classification - Class 1, General Controls

Product Code HPG Aid, Vision, Electronic, Battery-powered
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 886.5900
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.