Vista FS, Vista FS Liquid
K-Number: K190220 · 2019-06-10
Device Summary
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. The listed applicant is Inter-Med/Vista Dental Products. The 510(k) number is K190220.
When did Vista FS, Vista FS Liquid receive FDA 510(k) clearance?
Vista FS, Vista FS Liquid received FDA 510(k) clearance on 2019-06-10, under 510(k) number K190220.
Who is the listed applicant for Vista FS, Vista FS Liquid?
The FDA 510(k) record lists Inter-Med/Vista Dental Products as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Vista FS, Vista FS Liquid?
The FDA product code for Vista FS, Vista FS Liquid is MVL.
Other records listing Inter-Med/Vista Dental Products as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: MVL)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.