Bci, Inc. - FDA 510(k) Cleared Devices
13
Total
13
Cleared
0
Denied
Bci, Inc. has 13 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 13 cleared submissions from 1979 to 2003. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Bci, Inc. Filter by specialty or product code using the sidebar.
13 devices
Cleared
Aug 19, 2003
ADVISOR, MODEL 9200
Anesthesiology
193d
Cleared
Aug 18, 2003
BCI 6004 NIBP MONITOR WITH NELLCOR PULSE OXIMETER
Anesthesiology
75d
Cleared
Jun 03, 2002
BCI 3178 PEDIATRIC PULSE OXIMETRY SENSOR
Anesthesiology
89d
Cleared
Apr 30, 2002
BCI 3180 PULSE OXIMETER
Anesthesiology
85d
Cleared
Feb 21, 2002
BCI 1621 OXIMETRY DATA MANAGEMENT PROGRAM
Anesthesiology
92d
Cleared
Jan 03, 2002
3420 DIGIT PULSE OXIMETER, MODEL 3420
Anesthesiology
101d
Cleared
Jun 14, 2001
BCI 3403 SLEEP SCREENING PULSE OXIMETER
Anesthesiology
59d
Cleared
Jun 12, 2001
BCI ADVISOR VITAL SIGNS MONITOR (9200)
Cardiovascular
90d
Cleared
May 23, 2001
BCI ADVISOR VITAL SIGNS MONITOR (9200)
Cardiovascular
36d
Cleared
Jul 05, 2000
BCI M4529A OEM DIGITAL HANDHELD OXIMETER, MODEL M4529A
Anesthesiology
23d
Cleared
Jan 27, 1995
SHARPS CONTAINER 18 GALLON
General Hospital
157d
Cleared
Oct 17, 1994
CAPNOCHECK
Anesthesiology
175d
Cleared
Feb 15, 1979
IRRIGATOR, BODY CAVITY
General & Plastic Surgery
94d