NON-PRESCRIPTION SUNGLASSES— 510(k) K961990

Name: FDA 510(k) clearance K961990
Creator: U.S. Food and Drug Administration
Published: 1996-06-06

Substantially Equivalent

Rokko Stars Co., Ltd.

FDA 510(k) clearance K961990 for NON-PRESCRIPTION SUNGLASSES, Substantially Equivalent on 1996-06-06. Applicant: Rokko Stars Co., Ltd.. Device class: 1.

Clearance details

Applicant: Rokko Stars Co., Ltd.
Product code: Code HQY
Device class: Class 1
Regulation: 21 CFR 886.5850
Advisory panel: Ophthalmic
Date received: 1996-05-21
Decision date: 1996-06-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kobe, JP

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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.