FDA 510(k)

Adravision Perio

K-Number: K232440 · 2023-12-05

Decision Date2023-12-05

Product CodeQIH

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

Adravision Perio is the device name listed in this FDA 510(k) record. The listed applicant is Adra Corporation. It received FDA 510(k) clearance on 2023-12-05 under 510(k) number K232440. 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 Adravision Perio?

Adravision Perio is a medical device that received FDA 510(k) clearance on 2023-12-05. The listed applicant is Adra Corporation. The 510(k) number is K232440.

When did Adravision Perio receive FDA 510(k) clearance?

Adravision Perio received FDA 510(k) clearance on 2023-12-05, under 510(k) number K232440.

Who is the listed applicant for Adravision Perio?

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

What is the FDA product code for Adravision Perio?

The FDA product code for Adravision Perio is QIH.

Related Devices (Code: QIH)

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.

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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.