510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K202222Substantially Equivalent

Irrisept Wound Debridement and Cleansing System

IrriMAX Corporation, Lawrenceville GA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K202222 is the FDA 510(k) clearance record for Irrisept Wound Debridement and Cleansing System, a class II device, cleared for Irrimax Corporation on under FDA product code FQH (Lavage, Jet). FDA records list 5 510(k) clearances for Irrimax Corporation, from to . As of , FDA records show no recalls naming K202222.

Clearance record

Decision date
Received
(130 days to decision)
Product code
FQH Lavage, Jet
Regulation
21 CFR 880.5475
Device class
Class II
Review panel
General Hospital
Applicant
Irrimax Corporation 1665 Lakes Pkwy. - Suite 102, Lawrenceville GA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code FQH

Trailing 12 months
2 clearances under product code FQH in the twelve months to October 2026, February 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code FQH, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20262
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260