Vista Clear
K-Number: K193389 · 2020-03-04
ApplicantInter-Med/Vista Dental Products
Decision Date2020-03-04
Product CodeMVL
DecisionSubstantially Equivalent
Device Summary
Vista Clear is a medical device manufactured by Inter-Med/Vista Dental Products. It received FDA 510(k) clearance on 2020-03-04 under approval number K193389. The device is classified under product code MVL. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Vista Clear?
Vista Clear is a medical device that received FDA 510(k) clearance on 2020-03-04. It is manufactured by Inter-Med/Vista Dental Products. The 510(k) number is K193389.
When was Vista Clear approved by the FDA?
Vista Clear received FDA 510(k) clearance on 2020-03-04, under approval number K193389.
What company makes Vista Clear?
Vista Clear is manufactured by Inter-Med/Vista Dental Products.
What is the FDA product code for Vista Clear?
The FDA product code for Vista Clear is MVL.
Other Devices by Inter-Med/Vista Dental Products
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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.