Avid IF2
K-Number: K183692 · 2019-06-12
Decision Date2019-06-12
Product CodeLIH
Advisory CommitteeNE
DecisionSubstantially Equivalent
Device Summary
Avid IF2 is a medical device manufactured by Vision Quest Industries Inc./Dba VQ Orthocare. It received FDA 510(k) clearance on 2019-06-12 under approval number K183692. The device is classified under product code LIH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Avid IF2?
Avid IF2 is a medical device that received FDA 510(k) clearance on 2019-06-12. It is manufactured by Vision Quest Industries Inc./Dba VQ Orthocare. The 510(k) number is K183692.
When was Avid IF2 approved by the FDA?
Avid IF2 received FDA 510(k) clearance on 2019-06-12, under approval number K183692.
What company makes Avid IF2?
Avid IF2 is manufactured by Vision Quest Industries Inc./Dba VQ Orthocare.
What is the FDA product code for Avid IF2?
The FDA product code for Avid IF2 is LIH.
Other Devices by Vision Quest Industries Inc./Dba VQ Orthocare
Related Devices (Code: LIH)
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.