# Cardiopulmonary Corp.

- Location (FDA's records): Milford, CT
- FDA decisions: 9 (1995–2013): 9 510(k) clearances
- Product codes: MSX (3), CBK (3), MOD (2), MHX (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 7 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Innovision Medical Technologies, LLC: 1 (https://510kreport.com/company/innovision-medical-technologies)
- Covidien: 1 (https://510kreport.com/company/covidien)
- Philips Medical Systems, Inc.: 1 (https://510kreport.com/company/philips-medical-systems)
- Critical Alert: 1 (https://510kreport.com/company/critical-alert)
- Respironics, Inc.: 1 (https://510kreport.com/company/respironics)
- Masimo Corporation: 1 (https://510kreport.com/company/masimo)
- Sentec AG: 1 (https://510kreport.com/company/sentec)

## Its most-cited devices
- K061932: Bernoulli Management System (MS) Software (2006), cited by 2
- K011861: Bernoulli Ventilator Management System (2001), cited by 2
- K091461: Bernoulli Management System, Oxinet Iii and Lifegard Vue (2009), cited by 2
- K130208: Bernoulli Enterprise Software (2013), cited by 1

## Recent decisions
- K130208: Bernoulli Enterprise Software (Dec 20, 2013)
- K091461: Bernoulli Management System, Oxinet Iii and Lifegard Vue (Aug 14, 2009)
- K061932: Bernoulli Management System (MS) Software (Sep 14, 2006)
- K051283: Modification to Bernoulli Ventilator Management System Software (Jun 23, 2005)
- K020018: Modification to Bernoulli Ventilator Management System Software (Feb 21, 2002)
- K011861: Bernoulli Ventilator Management System (Nov 6, 2001)
- K990429: Modification of Venturi Ventilator (Feb 24, 1999)
- K982174: Venturi Ventilator (Jun 24, 1998)

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