EYEDENTITY EYEWEAR— 510(k) K851039

Name: FDA 510(k) clearance K851039
Creator: U.S. Food and Drug Administration
Published: 1985-04-01

Substantially Equivalent

Vitech Research C/O Johnsen, Manfredi & Thorpe

FDA 510(k) clearance K851039 for EYEDENTITY EYEWEAR, Substantially Equivalent on 1985-04-01. Applicant: Vitech Research C/O Johnsen, Manfredi & Thorpe. Device class: 1.

Clearance details

Applicant: Vitech Research C/O Johnsen, Manfredi & Thorpe
Product code: Code HQZ
Device class: Class 1
Regulation: 21 CFR 886.5842
Advisory panel: Ophthalmic
Date received: 1985-03-14
Decision date: 1985-04-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Los Angeles, CA, US

Download summary PDF View on FDA.gov ↗

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