PLASTIC FRAME & LENS SUNGLASS— 510(k) K881419

Name: FDA 510(k) clearance K881419
Creator: U.S. Food and Drug Administration
Published: 1988-05-25

Substantially Equivalent

Marketing Innovations Intl., Inc.

FDA 510(k) clearance K881419 for PLASTIC FRAME & LENS SUNGLASS, Substantially Equivalent on 1988-05-25. Applicant: Marketing Innovations Intl., Inc.. Device class: 1.

Clearance details

Applicant: Marketing Innovations Intl., Inc.
Product code: Code HQY
Device class: Class 1
Regulation: 21 CFR 886.5850
Advisory panel: Ophthalmic
Date received: 1988-04-04
Decision date: 1988-05-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Calabasas, CA, US

Download summary PDF View on FDA.gov ↗

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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.