Avid IF2— 510(k) K183692

Name: FDA 510(k) clearance K183692
Creator: U.S. Food and Drug Administration
Published: 2019-06-12

Substantially Equivalent

Vision Quest Industries Inc./Dba VQ Orthocare

FDA 510(k) clearance K183692 for Avid IF2, Substantially Equivalent on 2019-06-12. Applicant: Vision Quest Industries Inc./Dba VQ Orthocare. Device class: 2.

Clearance details

Applicant: Vision Quest Industries Inc./Dba VQ Orthocare
Product code: Code LIH
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 2018-12-31
Decision date: 2019-06-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Vista, CA, US

Download summary PDF View on FDA.gov ↗

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