ARISTAR EYEWEAR, ESPRIT EYEWEAR— 510(k) K945122

Name: FDA 510(k) clearance K945122
Creator: U.S. Food and Drug Administration
Published: 1994-11-22

Substantially Equivalent

Aristar Inc. U.S.A.

FDA 510(k) clearance K945122 for ARISTAR EYEWEAR, ESPRIT EYEWEAR, Substantially Equivalent on 1994-11-22. Applicant: Aristar Inc. U.S.A.. Device class: 1.

Clearance details

Applicant: Aristar Inc. U.S.A.
Product code: Code HQY
Device class: Class 1
Regulation: 21 CFR 886.5850
Advisory panel: Ophthalmic
Date received: 1994-10-19
Decision date: 1994-11-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Morris Plains, NJ, US

Download summary PDF View on FDA.gov ↗

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K945123 — ARISTAR EYEWEAR, ESPRIT EYEWEAR1994-11-22

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