VISOR SUNGLASSES/LENS/NOVELTY VISOR— 510(k) K915266

Name: FDA 510(k) clearance K915266
Creator: U.S. Food and Drug Administration
Published: 1992-09-02

Substantially Equivalent

Janlin Ent.

FDA 510(k) clearance K915266 for VISOR SUNGLASSES/LENS/NOVELTY VISOR, Substantially Equivalent on 1992-09-02. Applicant: Janlin Ent.. Device class: 1.

Clearance details

Applicant: Janlin Ent.
Product code: Code HQY
Device class: Class 1
Regulation: 21 CFR 886.5850
Advisory panel: Ophthalmic
Date received: 1991-11-20
Decision date: 1992-09-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Torrance, CA, US

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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.