K-number	K183692
Device name	Avid IF2
Applicant	Vision Quest Industries Inc./Dba VQ Orthocare
Product code	LIH
Device class	Class II
Decision date	Jun 12, 2019
Decision	Substantially Equivalent
Regulation	882.5890

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Source

View the full FDA submission: accessdata.fda.gov

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Avid IF2

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