THEO NON-PRESCRIPTION SUNGLASSES/SPECTACLE FRAMES— 510(k) K924938

Name: FDA 510(k) clearance K924938
Creator: U.S. Food and Drug Administration
Published: 1993-04-06

Substantially Equivalent

Eyeworks 3

FDA 510(k) clearance K924938 for THEO NON-PRESCRIPTION SUNGLASSES/SPECTACLE FRAMES, Substantially Equivalent on 1993-04-06. Applicant: Eyeworks 3. Device class: 1.

Clearance details

Applicant: Eyeworks 3
Product code: Code HQY
Device class: Class 1
Regulation: 21 CFR 886.5850
Advisory panel: Ophthalmic
Date received: 1992-09-30
Decision date: 1993-04-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Los Angeles, CA, 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

More clearances from Eyeworks 3

view all

K925736 — NON-PRES SUNGLASSES/SPEC FRAMES (PLASTIC & METAL)1993-06-28

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