Cleared Traditional

DAELIM CORP. EYE WEAR MODEL (K932612) - FDA 510(k) Clearance

Class I Ophthalmic device.

K932612 · Daelim Corp. · Ophthalmic device
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Apr 1994
Decision
313d
Days
Class 1
Risk

K932612 is an FDA 510(k) clearance for the DAELIM CORP. EYE WEAR MODEL. Classified as Frame, Spectacle (product code HQZ), Class I - General Controls.

Submitted by Daelim Corp. (Miami, US). The FDA issued a Cleared decision on April 6, 1994 after a review of 313 days - an unusually long review period, suggesting complex equivalence evaluation.

This device falls under the Ophthalmic FDA review panel, regulated under 21 CFR 886.5842 - 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. Elevated predicate reliance profile. 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 Daelim Corp. devices

Submission Details

510(k) Number K932612 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 28, 1993
Decision Date April 06, 1994
Days to Decision 313 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
203d slower than avg
Panel avg: 110d · This submission: 313d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code HQZ Frame, Spectacle
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 886.5842
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.