# Ferraris Respiratory, Inc.

- Location (FDA's records): Louisville, CO
- FDA decisions: 2 (1992–2002): 2 510(k) clearances
- Product codes: BZG (2)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 3 (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 whose devices it cites most
- Korr Medical Technologies, Inc.: 1 (https://510kreport.com/company/korr-medical-technologies)
- Schiller AG: 1 (https://510kreport.com/company/schiller)

## Firms that cite its devices most
- Pulmonary Data Services, Inc.: 2 (https://510kreport.com/company/pulmonary-data-services)
- Micro Direct, Inc.: 1 (https://510kreport.com/company/micro-direct)

## Its most-cited devices
- K914272: Koko Spirometer (1992), cited by 2
- K022276: Kokomate (2002), cited by 1

## Recent decisions
- K022276: Kokomate (Oct 4, 2002)
- K914272: Koko Spirometer (Jul 2, 1992)

Source page: https://510kreport.com/company/ferraris-respiratory