Cleared Traditional

THE NISSEL ARTIFICIAL EYE (K923167) - FDA 510(k) Clearance

Class I Ophthalmic device.

K923167 · Nissel , Ltd. · Ophthalmic device
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Sep 1992
Decision
65d
Days
Class 1
Risk

K923167 is an FDA 510(k) clearance for the THE NISSEL ARTIFICIAL EYE. Classified as Eye, Artificial, Non-custom (product code HQH), Class I - General Controls.

Submitted by Nissel , Ltd. (Chicago, US). The FDA issued a Cleared decision on September 2, 1992 after a review of 65 days - a notably fast clearance cycle.

This device falls under the Ophthalmic FDA review panel, regulated under 21 CFR 886.3200 - 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 Nissel , Ltd. devices

Submission Details

510(k) Number K923167 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 29, 1992
Decision Date September 02, 1992
Days to Decision 65 days
Submission Type Traditional
Review Panel Ophthalmic (OP)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
45d faster than avg
Panel avg: 110d · This submission: 65d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code HQH Eye, Artificial, Non-custom
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 886.3200
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.