510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K242255Substantially Equivalent

Qitexio® 4-Way Stopcock (QIT014)

Medex, Saint-Priest, FR / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K242255 is the FDA 510(k) clearance record for Qitexio® 4-Way Stopcock (QIT014), a class II device, cleared for Medex on under FDA product code FMG (Stopcock, I.V. Set). FDA records list 2 510(k) clearances for Medex, from to . As of , FDA records show no recalls naming K242255.

Clearance record

Decision date
Received
(272 days to decision)
Product code
FMG Stopcock, I.V. Set
Regulation
21 CFR 880.5440
Device class
Class II
Review panel
General Hospital
Applicant
Medex 240 Allee Jacques Monod, Saint-Priest, FR
510(k) summary
Summary PDF
Third party review
No

Clearances, product code FMG

Trailing 12 months

FDA records hold no clearances under product code FMG in the trailing twelve months.

FDA records show no clearances under product code FMG in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code FMG, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260