Cleared Traditional

K822917 - MODEL 5400 OPTOKINETIC STIMULATOR (FDA 510(k) Clearance)

Class I Ophthalmic device.

K822917 · Life-Tech Intl., Inc. · Ophthalmic device
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Nov 1982
Decision
31d
Days
Class 1
Risk

K822917 is an FDA 510(k) clearance for the MODEL 5400 OPTOKINETIC STIMULATOR. Classified as Drum, Opticokinetic (product code HOW), Class I - General Controls.

Submitted by Life-Tech Intl., Inc. (Mchenry, US). The FDA issued a Cleared decision on November 1, 1982 after a review of 31 days - a notably fast clearance cycle.

This device falls under the Ophthalmic FDA review panel, regulated under 21 CFR 886.1200 - 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 Life-Tech Intl., Inc. devices

Submission Details

510(k) Number K822917 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 01, 1982
Decision Date November 01, 1982
Days to Decision 31 days
Submission Type Traditional
Review Panel Ophthalmic (OP)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
79d faster than avg
Panel avg: 110d · This submission: 31d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code HOW Drum, Opticokinetic
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 886.1200
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.