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FDA 510(k)

Armis VeriCyn Wound Wash

K-Number: K220759 · 2023-05-25

ApplicantArmis Biopharma, Inc.
Decision Date2023-05-25
Product CodeFQH
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Armis VeriCyn Wound Wash is a medical device manufactured by Armis Biopharma, Inc.. It received FDA 510(k) clearance on 2023-05-25 under approval number K220759. The device is classified under product code FQH. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Armis VeriCyn Wound Wash?

Armis VeriCyn Wound Wash is a medical device that received FDA 510(k) clearance on 2023-05-25. It is manufactured by Armis Biopharma, Inc.. The 510(k) number is K220759.

When was Armis VeriCyn Wound Wash approved by the FDA?

Armis VeriCyn Wound Wash received FDA 510(k) clearance on 2023-05-25, under approval number K220759.

What company makes Armis VeriCyn Wound Wash?

Armis VeriCyn Wound Wash is manufactured by Armis Biopharma, Inc..

What is the FDA product code for Armis VeriCyn Wound Wash?

The FDA product code for Armis VeriCyn Wound Wash is FQH.

Other Devices by Armis Biopharma, Inc.

K202777VeriFixx™ Small Bone Implant

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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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