Ino Therapeutics, LLC/Dba Ikaria is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ino Therapeutics, LLC/Dba Ikaria - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
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