# Fms, Finapres Medical Systems BV

- Location (FDA's records): Santa Barbara, CA
- FDA decisions: 2 (2003–2003): 2 510(k) clearances
- Product codes: DXN (2)
- Predicates its devices cite: 6 (0 its own); citations of its devices by later devices: 6 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Ohio Medical Products: 2 (https://510kreport.com/company/ohio-medical-products)
- Ohmeda Medical: 2 (https://510kreport.com/company/ohmeda-medical)
- Cnsystems Medizintechnik GmbH: 2 (https://510kreport.com/company/cnsystems-medizintechnik)

## Firms that cite its devices most
- Finapres Medical Systems B.V.: 2 (https://510kreport.com/company/finapres-medical-systems)
- Cnoga Medical, Ltd.: 2 (https://510kreport.com/company/cnoga-medical)
- Bmeye B.V.: 1 (https://510kreport.com/company/bmeye)
- Caretaker Medical, LLC: 1 (https://510kreport.com/company/caretaker-medical)

## Its most-cited devices
- K023723: Finometer Noninvasive Hemodynamic Monitor, Model 1 (2003), cited by 3
- K023338: Portapres Ambulatory Continuous Non Invasive Blood Pressure Monitor,Model-2 (2003), cited by 3

## Recent decisions
- K023723: Finometer Noninvasive Hemodynamic Monitor, Model 1 (Oct 23, 2003)
- K023338: Portapres Ambulatory Continuous Non Invasive Blood Pressure Monitor,Model-2 (May 9, 2003)

Source page: https://510kreport.com/company/fms-finapres-medical-systems