Vista Rinse, Vista Rinse Plus
K-Number: K193409 · 2020-09-09
ApplicantInter-Med/Vista Dental Products
Decision Date2020-09-09
Product CodeKJJ
DecisionSubstantially Equivalent
Device Summary
Vista Rinse, Vista Rinse Plus is a medical device manufactured by Inter-Med/Vista Dental Products. It received FDA 510(k) clearance on 2020-09-09 under approval number K193409. The device is classified under product code KJJ. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Vista Rinse, Vista Rinse Plus?
Vista Rinse, Vista Rinse Plus is a medical device that received FDA 510(k) clearance on 2020-09-09. It is manufactured by Inter-Med/Vista Dental Products. The 510(k) number is K193409.
When was Vista Rinse, Vista Rinse Plus approved by the FDA?
Vista Rinse, Vista Rinse Plus received FDA 510(k) clearance on 2020-09-09, under approval number K193409.
What company makes Vista Rinse, Vista Rinse Plus?
Vista Rinse, Vista Rinse Plus is manufactured by Inter-Med/Vista Dental Products.
What is the FDA product code for Vista Rinse, Vista Rinse Plus?
The FDA product code for Vista Rinse, Vista Rinse Plus is KJJ.
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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.