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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 the device name listed in this FDA 510(k) record. The listed applicant is Armis Biopharma, Inc.. It received FDA 510(k) clearance on 2023-05-25 under 510(k) 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. The listed applicant is Armis Biopharma, Inc.. The 510(k) number is K220759.

When did Armis VeriCyn Wound Wash receive FDA 510(k) clearance?

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

Who is the listed applicant for Armis VeriCyn Wound Wash?

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

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

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

Other records listing Armis Biopharma, 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.

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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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