FDA 510(k)

Videa Perio Assist

K-Number: K223296 · 2023-02-06

Decision Date2023-02-06

Product CodeQIH

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

Videa Perio Assist is the device name listed in this FDA 510(k) record. The listed applicant is Videahealth, Inc.. It received FDA 510(k) clearance on 2023-02-06 under 510(k) number K223296. The device is classified under product code QIH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Videa Perio Assist?

Videa Perio Assist is a medical device that received FDA 510(k) clearance on 2023-02-06. The listed applicant is Videahealth, Inc.. The 510(k) number is K223296.

When did Videa Perio Assist receive FDA 510(k) clearance?

Videa Perio Assist received FDA 510(k) clearance on 2023-02-06, under 510(k) number K223296.

Who is the listed applicant for Videa Perio Assist?

The FDA 510(k) record lists Videahealth, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Videa Perio Assist?

The FDA product code for Videa Perio Assist is QIH.

Other records listing Videahealth, Inc. 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.

K251002Videa Dental AI K232384Videa Dental Assist K213795Videa Caries Assist

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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.