Air Liquide Healthcare America Corporation is one of 18365 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Air Liquide Healthcare America Corporation - FDA 510(k) Cleared Devic...
Recent clearances: Intelli-Ox, PURE CRYOGEN
2
Total
2
Cleared
0
Denied
Air Liquide Healthcare America Corporation has 2 FDA 510(k) cleared medical devices. Based in Houston, US.
Historical record: 2 cleared submissions from 2016 to 2017. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Air Liquide Healthcare America Corporation Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by K&L Gates Llp as regulatory consultant.
FDA 510(k) Regulatory Record - Air Liquide Healthcare America Corporation
2 devices