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FDA 510(k)

V-Mix

K-Number: K193357 · 2020-10-23

ApplicantInter-Med/Vista Dental Products
Decision Date2020-10-23
Product CodeKJJ
DecisionSubstantially Equivalent

Device Summary

V-Mix is a medical device manufactured by Inter-Med/Vista Dental Products. It received FDA 510(k) clearance on 2020-10-23 under approval number K193357. The device is classified under product code KJJ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the V-Mix?

V-Mix is a medical device that received FDA 510(k) clearance on 2020-10-23. It is manufactured by Inter-Med/Vista Dental Products. The 510(k) number is K193357.

When was V-Mix approved by the FDA?

V-Mix received FDA 510(k) clearance on 2020-10-23, under approval number K193357.

What company makes V-Mix?

V-Mix is manufactured by Inter-Med/Vista Dental Products.

What is the FDA product code for V-Mix?

The FDA product code for V-Mix is KJJ.

Other Devices by Inter-Med/Vista Dental Products

K170101Valiant Curing Light K190220Vista FS, Vista FS Liquid K193409Vista Rinse, Vista Rinse Plus K193447Vista Dyes K193389Vista Clear

Related Devices (Code: KJJ)

K160577PacEndo ChlorhexidinePac-Dent International, Inc. K153528PacEndo EDTAPac-Dent International, Inc. K162311Straumann PrefGelInstitut Straumann AG K173163ChlorCid, ChlorCid V, ChlorCid SurfUltradent Products, Inc. K193409Vista Rinse, Vista Rinse PlusInter-Med/Vista Dental Products K200330RC-Prime Root Canal Preparation CreamPac-Dent, Inc.

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.

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