Medical Device Manufacturer · US , Port Allen , LA

Ino Therapeutics, LLC/Dba Ikaria - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2011

Total

Cleared

Denied

Ino Therapeutics, LLC/Dba Ikaria has 2 FDA 510(k) cleared medical devices. Based in Port Allen, US.

Historical record: 2 cleared submissions from 2011 to 2012. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Ino Therapeutics, LLC/Dba Ikaria Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Ino Therapeutics, LLC/Dba Ikaria

2 devices

1-2 of 2