Medex, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medex, Inc. - FDA 510(k) Cleared Devices
48
Total
46
Cleared
0
Denied
Medex, Inc. has 46 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 46 cleared submissions from 1977 to 2005. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Medex, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Medex, Inc.
48 devices
Cleared
Jan 04, 2005
PHARMGUARD TOOLBOX, MODEL G6000782
General Hospital
118d
Cleared
Apr 30, 2004
MEDEX 3000 SERIES MR SYRINGE INFUSION PUMP
General Hospital
24d
Cleared
May 20, 2002
TRANSTAR INTRACRANIAL PRESSURE TRANSDUCER, MODEL MX950ICP
Neurology
70d
Cleared
May 09, 2000
MEDEX 3000 SERIES MRI COMPATIBLE SYRINGE INFUSION PUMP
General Hospital
97d
Cleared
Apr 06, 1999
MEDEX 3000 SERIES SYRINGE INFUSION PUMP
General Hospital
251d
Cleared
Jul 21, 1998
CONTRAST CONTROL DEVICE
General Hospital
35d
Cleared
Jul 18, 1996
MEDFUSION MODEL 2001 SYRINGE INFUSION PUMP
General Hospital
247d
Cleared
Jun 27, 1996
MX960 REUSABLE PRESSURE TRANSDUCER
Cardiovascular
77d
Cleared
Jun 06, 1996
MX703 AND MX730 CONTINUOUS FLUSH DEVICES
Cardiovascular
45d
Cleared
Apr 22, 1996
STOPCOCK & LUER LOCK PLUG
General Hospital
175d
Cleared
Sep 21, 1995
INTRAVASCULAR (I-V) ADMININISTRATION SET (DVGENPERS FPA)
General Hospital
136d
Cleared
Apr 05, 1995
NOVATRANS II
Cardiovascular
23d
Looking for a specific device from Medex, Inc.? Search by device name or K-number.
Search all Medex, Inc. devices