Linde Gas Therapeutics is one of 18344 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Linde Gas Therapeutics - FDA 510(k) Cleared Devices
Recent clearances: HELONTIX VENT, LINDE INTEGRATED VALVE (LIV)
2
Total
2
Cleared
0
Denied
Linde Gas Therapeutics has 2 FDA 510(k) cleared medical devices. Based in Broadview Heights, US.
Historical record: 2 cleared submissions from 2007 to 2008. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Linde Gas Therapeutics Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Linde Gas Therapeutics
2 devices