K-number	K202490
Device name	Avid CT2
Applicant	Vision Quest Industries Inc./Dba VQ Orthocare
Product code	IPF
Device class	Class II
Decision date	Nov 16, 2020
Decision	Substantially Equivalent
Regulation	890.5850

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Source

View the full FDA submission: accessdata.fda.gov

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Avid CT2

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