MYVISIONTRACK(TM)— 510(k) K121738

Name: FDA 510(k) clearance K121738
Creator: U.S. Food and Drug Administration
Published: 2013-02-22

Substantially Equivalent

Vital Art and Science Incorporated

FDA 510(k) clearance K121738 for MYVISIONTRACK(TM), Substantially Equivalent on 2013-02-22. Applicant: Vital Art and Science Incorporated. Device class: 1.

Clearance details

Applicant: Vital Art and Science Incorporated
Product code: Code HOQ
Device class: Class 1
Regulation: 21 CFR 886.1330
Advisory panel: Ophthalmic
Date received: 2012-06-13
Decision date: 2013-02-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Richardson, TX, US

Download summary PDF View on FDA.gov ↗

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