FDA 510(k) Applications Submitted by BCI, INC.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K020350 |
02/04/2002 |
BCI 3180 PULSE OXIMETER |
BCI, INC. |
| K030407 |
02/07/2003 |
ADVISOR, MODEL 9200 |
BCI, INC. |
| K010770 |
03/14/2001 |
BCI ADVISOR VITAL SIGNS MONITOR (9200) |
BCI, INC. |
| K011156 |
04/16/2001 |
BCI 3403 SLEEP SCREENING PULSE OXIMETER |
BCI, INC. |
| K001770 |
06/12/2000 |
BCI M4529A OEM DIGITAL HANDHELD OXIMETER, MODEL M4529A |
BCI, INC. |
| K013171 |
09/24/2001 |
3420 DIGIT PULSE OXIMETER, MODEL 3420 |
BCI, INC. |
| K013862 |
11/21/2001 |
BCI 1621 OXIMETRY DATA MANAGEMENT PROGRAM |
BCI, INC. |
| K020739 |
03/06/2002 |
BCI 3178 PEDIATRIC PULSE OXIMETRY SENSOR |
BCI, INC. |
| K011177 |
04/17/2001 |
BCI ADVISOR VITAL SIGNS MONITOR (9200) |
BCI, INC. |
| K031742 |
06/04/2003 |
BCI 6004 NIBP MONITOR WITH NELLCOR PULSE OXIMETER |
BCI, INC. |
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