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FDA 510(k)

Vista Rinse, Vista Rinse Plus

K-Number: K193409 · 2020-09-09

Decision Date2020-09-09
Product CodeKJJ
DecisionSubstantially Equivalent

Device Summary

Vista Rinse, Vista Rinse Plus 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 2020-09-09 under 510(k) 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. The listed applicant is Inter-Med/Vista Dental Products. The 510(k) number is K193409.

When did Vista Rinse, Vista Rinse Plus receive FDA 510(k) clearance?

Vista Rinse, Vista Rinse Plus received FDA 510(k) clearance on 2020-09-09, under 510(k) number K193409.

Who is the listed applicant for Vista Rinse, Vista Rinse Plus?

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 Rinse, Vista Rinse Plus?

The FDA product code for Vista Rinse, Vista Rinse Plus 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.

Related Devices (Code: KJJ)

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

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