Avid CT2
K-Number: K202490 · 2020-11-16
Decision Date2020-11-16
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent
Device Summary
Avid CT2 is a medical device manufactured by Vision Quest Industries Inc./Dba VQ Orthocare. It received FDA 510(k) clearance on 2020-11-16 under approval number K202490. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Avid CT2?
Avid CT2 is a medical device that received FDA 510(k) clearance on 2020-11-16. It is manufactured by Vision Quest Industries Inc./Dba VQ Orthocare. The 510(k) number is K202490.
When was Avid CT2 approved by the FDA?
Avid CT2 received FDA 510(k) clearance on 2020-11-16, under approval number K202490.
What company makes Avid CT2?
Avid CT2 is manufactured by Vision Quest Industries Inc./Dba VQ Orthocare.
What is the FDA product code for Avid CT2?
The FDA product code for Avid CT2 is IPF.
Other Devices by Vision Quest Industries Inc./Dba VQ Orthocare
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.