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Bci, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
13
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K030407ADVISOR, MODEL 9200August 19, 2003
K031742BCI 6004 NIBP MONITOR WITH NELLCOR PULSE OXIMETERAugust 18, 2003
K020739BCI 3178 PEDIATRIC PULSE OXIMETRY SENSORJune 3, 2002
K020350BCI 3180 PULSE OXIMETERApril 30, 2002
K013862BCI 1621 OXIMETRY DATA MANAGEMENT PROGRAMFebruary 21, 2002
K0131713420 DIGIT PULSE OXIMETER, MODEL 3420January 3, 2002
K011156BCI 3403 SLEEP SCREENING PULSE OXIMETERJune 14, 2001
K010770BCI ADVISOR VITAL SIGNS MONITOR (9200)June 12, 2001
K011177BCI ADVISOR VITAL SIGNS MONITOR (9200)May 23, 2001
K001770BCI M4529A OEM DIGITAL HANDHELD OXIMETER, MODEL M4529AJuly 5, 2000
K944121SHARPS CONTAINER 18 GALLONJanuary 27, 1995
K941982CAPNOCHECKOctober 17, 1994
K781918IRRIGATOR, BODY CAVITYFebruary 15, 1979