OPTICAL ACCESSORIES-SPECTACLE FRAMES AND SUNGLASSES— 510(k) K932125

Name: FDA 510(k) clearance K932125
Creator: U.S. Food and Drug Administration
Published: 1993-10-01

Substantially Equivalent

Vision Design Eyewear, Inc.

FDA 510(k) clearance K932125 for OPTICAL ACCESSORIES-SPECTACLE FRAMES AND SUNGLASSES, Substantially Equivalent on 1993-10-01. Applicant: Vision Design Eyewear, Inc.. Device class: 1.

Clearance details

Applicant: Vision Design Eyewear, Inc.
Product code: Code HQZ
Device class: Class 1
Regulation: 21 CFR 886.5842
Advisory panel: Ophthalmic
Date received: 1993-05-03
Decision date: 1993-10-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Miami, FL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HQZ

view all

K952597 — VIEW POINT, DORION, RUDDY PROJECT, ULTRA FLEX, TRILLON, BAY BOY, SHIELD SKI, SUN POCKETS, POINT OF VIEW1995-09-12
K944313 — SPECTACLE FRAME1995-03-28
K945176 — SPECTACLE FRAME OR EYEGLASS FRAMES1994-12-15
K945392 — SPECTACLE FRAME1994-12-15
K945770 — OPTICAL FRAMES1994-12-15

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