Marquest Medical Products, Inc. - FDA 510(k) Cleared Devices
32
Total
32
Cleared
0
Denied
Marquest Medical Products, Inc. has 32 FDA 510(k) cleared anesthesiology devices. Based in Englewood, US.
Historical record: 32 cleared submissions from 1980 to 2005.
Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
32 devices
Cleared
Mar 01, 2005
C-CO2 COLORIMETRIC CO2 INDICATOR
Anesthesiology
48d
Cleared
Jul 16, 1997
SCT 3000 HEATED HUMIDIFIER
Anesthesiology
159d
Cleared
Jan 14, 1997
HEATED WIRE CIRCUITS FOR SCT 3000 HEATED HUMIDIFIER
Anesthesiology
218d
Cleared
Jan 14, 1997
WATER CHAMBERS FOR ST 3000 HEATED HUMIDIFIER
Anesthesiology
218d
Cleared
Oct 18, 1996
DISPOSABLE GAS SAMPLING INTERFACE KITS
Anesthesiology
221d
Cleared
Oct 18, 1996
RESPIRGARD II, SPIROGARD
General Hospital
158d
Cleared
Feb 01, 1991
TEMP MARQ(TM) CONVECTIVE WARMING SYSTEM
Cardiovascular
108d
Cleared
Oct 11, 1990
MARQUEST SCT 3000, HEATED HUMIDIFICATION SYSTEM
Anesthesiology
86d
Cleared
Sep 04, 1990
GAS-LYTE 1CC AND 3CC ARTERIAL BLOOD SAMPLERS
Anesthesiology
82d
Cleared
Aug 17, 1990
TEMP MARQ TEMPERATURE TREND INDICATOR
General Hospital
24d
Cleared
Jul 15, 1988
MARQUEST SCT 2000, HEATED HUMIDIFICATION SYSTEM
Anesthesiology
129d
Cleared
Dec 21, 1987
RESPIRGARD II NEBULIZER SYSTEM
Anesthesiology
54d