Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Irrisept Antimicrobial Wound Lavage

K-Number: K222804 · 2022-09-22

Decision Date2022-09-22
Product CodeFQH
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Irrisept Antimicrobial Wound Lavage is a medical device manufactured by Irrimax Corporation. It received FDA 510(k) clearance on 2022-09-22 under approval number K222804. 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 Irrisept Antimicrobial Wound Lavage?

Irrisept Antimicrobial Wound Lavage is a medical device that received FDA 510(k) clearance on 2022-09-22. It is manufactured by Irrimax Corporation. The 510(k) number is K222804.

When was Irrisept Antimicrobial Wound Lavage approved by the FDA?

Irrisept Antimicrobial Wound Lavage received FDA 510(k) clearance on 2022-09-22, under approval number K222804.

What company makes Irrisept Antimicrobial Wound Lavage?

Irrisept Antimicrobial Wound Lavage is manufactured by Irrimax Corporation.

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 PubMed Literature

Other Devices by Irrimax Corporation

Related Devices (Code: FQH)

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.