Medex, Inc. - FDA 510(k) Cleared Devices
Recent clearances: PHARMGUARD TOOLBOX, MODEL G6000782, MEDEX 3000 SERIES MR SYRINGE INFUSION PUMP, TRANSTAR INTRACRANIAL PRESSURE TRANSDUCER, MODEL MX950ICP
48
Total
46
Cleared
0
Denied
FDA 510(k) Regulatory Record - Medex, Inc. Cardiovascular ✕
19 devices
Cleared
Jun 27, 1996
MX960 REUSABLE PRESSURE TRANSDUCER
Cardiovascular
77d
Cleared
Jun 06, 1996
MX703 AND MX730 CONTINUOUS FLUSH DEVICES
Cardiovascular
45d
Cleared
Apr 05, 1995
NOVATRANS II
Cardiovascular
23d
Cleared
Aug 16, 1994
TRANSTAR PRESSURE TRANSDUCER
Cardiovascular
90d
Cleared
Aug 11, 1994
MEDFLATOR II(TM) DISPOSABLE INFLATION DEVICE
Cardiovascular
168d
Cleared
Sep 11, 1991
MX 339 TWIN HEMOSTATIC Y CONNECTOR
Cardiovascular
84d
Cleared
Jul 12, 1991
MEDFLATOR INFLATION SYSTEM
Cardiovascular
128d
Cleared
Dec 27, 1990
CENTRAL VENOUS PRESSURE MANOMETER
Cardiovascular
76d
Cleared
Dec 17, 1990
HOLLOW LUMEN NEEDLE, PART NUMBER: MX920
Cardiovascular
150d
Cleared
Nov 05, 1990
ARTERIAL BLOOD SAMPLING KIT
Cardiovascular
137d
Cleared
Sep 12, 1988
MX860, REUSABLE PRESSURE TRANSDUCER
Cardiovascular
52d
Cleared
Jun 15, 1988
MX1002 CABLE-CAL TM
Cardiovascular
114d