# Bci, Inc.

- Location (FDA's records): Waukesha, WI
- FDA decisions: 13 (1979–2003): 13 510(k) clearances
- Product codes: DQA (7), CCK (2), FMI (1), MWI (1), DPS (1), EYN (1)
- Predicates its devices cite: 21 (3 its own); citations of its devices by later devices: 6 (3 its own)
- Recalls linked to its devices: 47 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Bci Intl., Inc.: 9 (https://510kreport.com/company/bci-intl)
- Biochem International, Inc.: 4 (https://510kreport.com/company/biochem-international)
- Nellcor Puritan Bennett, Inc.: 3 (https://510kreport.com/company/nellcor-puritan-bennett)
- Nonin Medical, Inc.: 2 (https://510kreport.com/company/nonin-medical)

## Firms that cite its devices most
- Solaris Medical Technology, Inc.: 1 (https://510kreport.com/company/solaris-medical-technology)
- Bci Intl., Inc.: 1 (https://510kreport.com/company/bci-intl)
- Mir Medical Intl. Research Srl: 1 (https://510kreport.com/company/mir-medical-intl-research)

## Its most-cited devices
- K010770: Bci Advisor Vital Signs Monitor (9200) (2001), cited by 1
- K011156: Bci 3403 Sleep Screening Pulse Oximeter (2001), cited by 1
- K030407: Advisor, Model 9200 (2003), cited by 1
- K011177: Bci Advisor Vital Signs Monitor (9200) (2001), cited by 1
- K013171: 3420 Digit Pulse Oximeter, Model 3420 (2002), cited by 1
- K941982: Capnocheck (1994), cited by 1

## Recent decisions
- K030407: Advisor, Model 9200 (Aug 19, 2003)
- K031742: Bci 6004 Nibp Monitor with Nellcor Pulse Oximeter (Aug 18, 2003)
- K020739: Bci 3178 Pediatric Pulse Oximetry Sensor (Jun 3, 2002)
- K020350: Bci 3180 Pulse Oximeter (Apr 30, 2002)
- K013862: Bci 1621 Oximetry Data Management Program (Feb 21, 2002)
- K013171: 3420 Digit Pulse Oximeter, Model 3420 (Jan 3, 2002)
- K011156: Bci 3403 Sleep Screening Pulse Oximeter (Jun 14, 2001)
- K010770: Bci Advisor Vital Signs Monitor (9200) (Jun 12, 2001)

Source page: https://510kreport.com/company/bci