REVERT SUNGLASSES & POLAR SUNGLASSES— 510(k) K953920

Name: FDA 510(k) clearance K953920
Creator: U.S. Food and Drug Administration
Published: 1995-09-12

Substantially Equivalent

Bella Occhiali, Inc.

FDA 510(k) clearance K953920 for REVERT SUNGLASSES & POLAR SUNGLASSES, Substantially Equivalent on 1995-09-12. Applicant: Bella Occhiali, Inc.. Device class: 1.

Clearance details

Applicant: Bella Occhiali, Inc.
Product code: Code HQY
Device class: Class 1
Regulation: 21 CFR 886.5850
Advisory panel: Ophthalmic
Date received: 1995-08-21
Decision date: 1995-09-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Merrick, NY, US

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