Vista FS, Vista FS Liquid
K-Number: K190220 · 2019-06-10
ApplicantInter-Med/Vista Dental Products
Decision Date2019-06-10
Product CodeMVL
DecisionSubstantially Equivalent
Device Summary
Vista FS, Vista FS Liquid is a medical device manufactured by Inter-Med/Vista Dental Products. It received FDA 510(k) clearance on 2019-06-10 under approval number K190220. The device is classified under product code MVL. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Vista FS, Vista FS Liquid?
Vista FS, Vista FS Liquid is a medical device that received FDA 510(k) clearance on 2019-06-10. It is manufactured by Inter-Med/Vista Dental Products. The 510(k) number is K190220.
When was Vista FS, Vista FS Liquid approved by the FDA?
Vista FS, Vista FS Liquid received FDA 510(k) clearance on 2019-06-10, under approval number K190220.
What company makes Vista FS, Vista FS Liquid?
Vista FS, Vista FS Liquid is manufactured by Inter-Med/Vista Dental Products.
What is the FDA product code for Vista FS, Vista FS Liquid?
The FDA product code for Vista FS, Vista FS Liquid is MVL.
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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.