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 the device name listed in this FDA 510(k) record. The listed applicant is Inter-Med/Vista Dental Products. It received FDA 510(k) clearance on 2020-10-23 under 510(k) 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. The listed applicant is Inter-Med/Vista Dental Products. The 510(k) number is K193357.

When did V-Mix receive FDA 510(k) clearance?

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

Who is the listed applicant for V-Mix?

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 V-Mix?

The FDA product code for V-Mix is KJJ.

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.

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

Related Devices (Code: KJJ)

K250279RC-SwiftPrepBelport Company, Inc., Gingi-Pak K241354Sealer SolventInter-Med, Inc.K201785EPIEN Dental CleanserEpien Medical, Inc.K211813TritonInter-Med / Vista Dental K193409Vista Rinse, Vista Rinse PlusInter-Med/Vista Dental Products K200330RC-Prime Root Canal Preparation CreamPac-Dent, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.