Medical Device Manufacturer · US , Louisville , CO

Ferraris Respiratory, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1992

Total

Cleared

Denied

Ferraris Respiratory, Inc. has 2 FDA 510(k) cleared medical devices. Based in Louisville, US.

Historical record: 2 cleared submissions from 1992 to 2002. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Ferraris Respiratory, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Ferraris Respiratory, Inc.

2 devices

1-2 of 2