Irrisept Antimicrobial Wound Lavage

Lavage, Jet

Irrimax Corporation

The following data is part of a premarket notification filed by Irrimax Corporation with the FDA for Irrisept Antimicrobial Wound Lavage.

Pre-market Notification Details

Device IDK222804
510k NumberK222804
Device Name:Irrisept Antimicrobial Wound Lavage
ClassificationLavage, Jet
Applicant Irrimax Corporation 1665 Lakes Parkway, Suite 102 Lawrenceville,  GA  30043
ContactTanya Eberle
CorrespondentTanya Eberle
Irrimax Corporation 1665 Lakes Parkway, Suite 102 Lawrenceville,  GA  30043
Product CodeFQH  
CFR Regulation Number880.5475 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeSpecial
3rd Party ReviewedNo
Combination ProductYes
Date Received2022-09-16
Decision Date2022-09-22

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
00842351120026 K222804 000
00842351120040 K222804 000

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