Vista Clear
K-Number: K193389 · 2020-03-04
Device Summary
Frequently Asked Questions
What is the Vista Clear?
Vista Clear is a medical device that received FDA 510(k) clearance on 2020-03-04. The listed applicant is Inter-Med/Vista Dental Products. The 510(k) number is K193389.
When did Vista Clear receive FDA 510(k) clearance?
Vista Clear received FDA 510(k) clearance on 2020-03-04, under 510(k) number K193389.
Who is the listed applicant for Vista Clear?
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 Clear?
The FDA product code for Vista Clear 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.