Cleared Traditional

K960798 - D & K SUNGLASSES

K960798 is an FDA 510(k) clearance for D & K SUNGLASSES, manufactured by D&K Stores, Inc.. The device is a Class 1 Ophthalmic device with product code HQY cleared through the Traditional 510(k) pathway after a 57-day FDA review.

K960798 · D&K Stores, Inc. · Ophthalmic device
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Apr 1996
Decision
57d
Days
Class 1
Risk

K960798 is an FDA 510(k) clearance for the D & K SUNGLASSES. Classified as Sunglasses (non-prescription Including Photosensitive) (product code HQY), Class I - General Controls.

Submitted by D&K Stores, Inc. (Oakhurst, US). The FDA issued a Cleared decision on April 24, 1996 after a review of 57 days - a notably fast clearance cycle.

This device falls under the Ophthalmic FDA review panel, regulated under 21 CFR 886.5850 - 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.

FDA 510(k) Submission Details - K960798

510(k) Number K960798 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 27, 1996
Decision Date April 24, 1996
Days to Decision 57 days
Submission Type Traditional
Review Panel Ophthalmic (OP)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
53d faster than avg
Panel avg: 110d · This submission: 57d
Pathway characteristics
Predicate-based equivalence.

HQY Device Classification - Class 1, General Controls

Product Code HQY Sunglasses (non-prescription Including Photosensitive)
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 886.5850
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.

Regulatory Peers - HQY Sunglasses (non-prescription Including Photosensitive)

All 605
Devices cleared under the same product code (HQY) and FDA review panel - the closest regulatory comparables to K960798.
TINY TOON SUNGLASSES & CABBAGE PATCH KIDS SUNGLASSES
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SUN CLIP
K961603 · Intromark, Inc. · May 1996
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K943145 · The Monticello Group, Inc. · Apr 1996
SUNGLASSES
K961034 · Kylie Enterprise Co. , Ltd. · Apr 1996
VISARD SUNGLASSES
K961117 · Visard Srl · Apr 1996
SUNGLASSES
K961128 · Vision-Pro Industrial, Ltd. · Apr 1996
K960798 · D & K SUNGLASSES
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