Irrisept Antimicrobial Wound Lavage
K-Number: K222804 · 2022-09-22
Device Summary
Frequently Asked Questions
What is the Irrisept Antimicrobial Wound Lavage?
Irrisept Antimicrobial Wound Lavage is a medical device that received FDA 510(k) clearance on 2022-09-22. The listed applicant is Irrimax Corporation. The 510(k) number is K222804.
When did Irrisept Antimicrobial Wound Lavage receive FDA 510(k) clearance?
Irrisept Antimicrobial Wound Lavage received FDA 510(k) clearance on 2022-09-22, under 510(k) number K222804.
Who is the listed applicant for Irrisept Antimicrobial Wound Lavage?
The FDA 510(k) record lists Irrimax Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Irrisept Antimicrobial Wound Lavage?
The FDA product code for Irrisept Antimicrobial Wound Lavage is FQH.
Related Clinical Trials
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.
Other records listing Irrimax Corporation 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.
Related Devices (Code: FQH)
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.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.