SUNGLASSES, NON PRESCRIPTION— 510(k) K920672

Name: FDA 510(k) clearance K920672
Creator: U.S. Food and Drug Administration
Published: 1992-11-23

Substantially Equivalent

Daystone Intl. Corp.

FDA 510(k) clearance K920672 for SUNGLASSES, NON PRESCRIPTION, Substantially Equivalent on 1992-11-23. Applicant: Daystone Intl. Corp.. Device class: 1.

Clearance details

Applicant: Daystone Intl. Corp.
Product code: Code HQY
Device class: Class 1
Regulation: 21 CFR 886.5850
Advisory panel: Ophthalmic
Date received: 1992-02-14
Decision date: 1992-11-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Dallas, TX, US

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.