Ferraris Respiratory, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Ferraris Respiratory, Inc. makes
Ferraris Respiratory, Inc. manufactures the KOKO Spirometer, a device for measuring lung function and airflow, and the KOKOMATE, a companion tool for monitoring and analyzing spirometry results.
These products are classified as Class II devices under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Koko Spirometer Ref K914272
Regimes: 510(k) Registry: 510(k)Kokomate Ref K022276
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ferraris Respiratory, Inc. have in the registry?
The registry currently lists 2 devices for Ferraris Respiratory, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ferraris Respiratory, Inc.'s devices?
Among its 2 most recently registered devices, Ferraris Respiratory, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Ferraris Respiratory, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Ferraris Respiratory, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ferraris Respiratory, Inc. in the registry?
The most recently registered devices listed for Ferraris Respiratory, Inc. include KOKO SPIROMETER and KOKOMATE.