ALL KINDS OF SUNGLASSES— 510(k) K853921

Name: FDA 510(k) clearance K853921
Creator: U.S. Food and Drug Administration
Published: 1985-10-15

Substantially Equivalent

Winsburn Company , Ltd.

FDA 510(k) clearance K853921 for ALL KINDS OF SUNGLASSES, Substantially Equivalent on 1985-10-15. Applicant: Winsburn Company , Ltd.. Device class: 1.

Clearance details

Applicant: Winsburn Company , Ltd.
Product code: Code HQY
Device class: Class 1
Regulation: 21 CFR 886.5850
Advisory panel: Ophthalmic
Date received: 1985-09-23
Decision date: 1985-10-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Republic Of China, TW

Download summary PDF View on FDA.gov ↗

Recent devices under product code HQY

view all

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.