Cleared Traditional

STRIPE PROJECTOR (K902138) - FDA 510(k) Clearance

Class I Ophthalmic device.

K902138 · Academic Catalyst Corp. · Ophthalmic device
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Jul 1990
Decision
56d
Days
Class 1
Risk

K902138 is an FDA 510(k) clearance for the STRIPE PROJECTOR. Classified as Lens, Fundus, Hruby, Diagnostic (product code HJI), Class I - General Controls.

Submitted by Academic Catalyst Corp. (Valhalla, US). The FDA issued a Cleared decision on July 5, 1990 after a review of 56 days - a notably fast clearance cycle.

This device falls under the Ophthalmic FDA review panel, regulated under 21 CFR 886.1395 - 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.

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Submission Details

510(k) Number K902138 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 10, 1990
Decision Date July 05, 1990
Days to Decision 56 days
Submission Type Traditional
Review Panel Ophthalmic (OP)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
54d faster than avg
Panel avg: 110d · This submission: 56d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code HJI Lens, Fundus, Hruby, Diagnostic
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 886.1395
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.