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Medex, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
50
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K242255Qitexio® 4-Way Stopcock (QIT014)April 29, 2025
K203738QitexioMarch 14, 2022
K042432PHARMGUARD TOOLBOX, MODEL G6000782January 4, 2005
K040899MEDEX 3000 SERIES MR SYRINGE INFUSION PUMPApril 30, 2004
K020780TRANSTAR INTRACRANIAL PRESSURE TRANSDUCER, MODEL MX950ICPMay 20, 2002
K000328MEDEX 3000 SERIES MRI COMPATIBLE SYRINGE INFUSION PUMPMay 9, 2000
K982640MEDEX 3000 SERIES SYRINGE INFUSION PUMPApril 6, 1999
K982123CONTRAST CONTROL DEVICEJuly 21, 1998
K955231MEDFUSION MODEL 2001 SYRINGE INFUSION PUMPJuly 18, 1996
K961404MX960 REUSABLE PRESSURE TRANSDUCERJune 27, 1996
K961527MX703 AND MX730 CONTINUOUS FLUSH DEVICESJune 6, 1996
K954970STOPCOCK & LUER LOCK PLUGApril 22, 1996
K952160INTRAVASCULAR (I-V) ADMININISTRATION SET (DVGENPERS FPA)September 21, 1995
K951129NOVATRANS IIApril 5, 1995
K943897NU-SITEFebruary 10, 1995
K944208IV ADMINISTRATION SET FPADecember 13, 1994
K942377TRANSTAR PRESSURE TRANSDUCERAugust 16, 1994
K940896MEDFLATOR II(TM) DISPOSABLE INFLATION DEVICEAugust 11, 1994
K922323MX4042/MC4044 SERIES SIMULCATH(TM)June 14, 1994
K913498MX927 BLOOD TRANSFER DEVICENovember 27, 1991