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FDA 510(k)

Adravision Perio

K-Number: K232440 · 2023-12-05

ApplicantAdra Corporation
Decision Date2023-12-05
Product CodeQIH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Adravision Perio is a medical device manufactured by Adra Corporation. It received FDA 510(k) clearance on 2023-12-05 under approval 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. It is manufactured by Adra Corporation. The 510(k) number is K232440.

When was Adravision Perio approved by the FDA?

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

What company makes Adravision Perio?

Adravision Perio is manufactured by Adra Corporation.

What is the FDA product code for Adravision Perio?

The FDA product code for Adravision Perio is QIH.

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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.

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