KUO & YANG SUNGLASSES— 510(k) K955290

Name: FDA 510(k) clearance K955290
Creator: U.S. Food and Drug Administration
Published: 1995-12-06

Substantially Equivalent

Kuo & Yang Industrial Co., Ltd.

FDA 510(k) clearance K955290 for KUO & YANG SUNGLASSES, Substantially Equivalent on 1995-12-06. Applicant: Kuo & Yang Industrial Co., Ltd.. Device class: 1.

Clearance details

Applicant: Kuo & Yang Industrial Co., Ltd.
Product code: Code HQY
Device class: Class 1
Regulation: 21 CFR 886.5850
Advisory panel: Ophthalmic
Date received: 1995-11-17
Decision date: 1995-12-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wood Dale, IL, US

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Recent devices under product code HQY

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K974852 — NON-PRESCRIPTION SUNGLASSES1998-01-30
K974860 — NON-PRESCRIPTION SUNGLASSES1998-01-30
K974861 — NON-PRESCRIPTION SUNGLASSES1998-01-27
K974511 — SUNGLASSES1998-01-12
K974441 — SUNGLASSES1998-01-09

Data sourced from openFDA. This site is unofficial and independent of the FDA.