Bio-Med Devices, Inc. - FDA 510(k) Cleared Devices
14
Total
13
Cleared
0
Denied
Bio-Med Devices, Inc. has 13 FDA 510(k) cleared anesthesiology devices. Based in Mchenry, US.
Last cleared in 2022. Active since 1980.
Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Bio-Med Devices, Inc.
14 devices
Cleared
Mar 17, 2022
OxyMinder
Anesthesiology
90d
Cleared
Jul 20, 2018
TV-100
Anesthesiology
203d
Cleared
Sep 19, 1995
CROSSVENT-4 VENTILATOR
Anesthesiology
454d
Cleared
Feb 12, 1990
IC-2A MRI ADULT/PEDIATRIC VENTILATOR
Anesthesiology
98d
Cleared
Feb 12, 1990
MVP-10 MRI INFANT VENTILATOR
Anesthesiology
98d
Cleared
Jan 22, 1988
CBG CUFF MANOMETER
Anesthesiology
136d
Cleared
Jun 05, 1987
M-1 PRESSURE MONITOR
Anesthesiology
63d
Cleared
Jun 05, 1987
M-2 OXYGEN/TEMPERATURE MONITOR
Anesthesiology
63d
Cleared
Apr 21, 1987
M-10 VENTILATION MONITOR
Anesthesiology
29d
Cleared
Feb 09, 1983
PROGRAMMABLE VENTILATOR
Anesthesiology
12d
Cleared
Feb 07, 1983
ET-3 EMERGENCY TRANSPORT VENTILATOR
Anesthesiology
47d
Cleared
Dec 09, 1981
IC-5 VENTILATOR
Anesthesiology
20d