Edwards Lifescience, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Edwards Lifescience, LLC - FDA 510(k) Cleared Devices
Recent clearances: PediaSat Oximetry Catheter, PreSep Oligon Oximetry Catheter, Edwards Oximetry Central Venous Catheter (previously PreSep Oximetry Catheter)
1
Total
1
Cleared
0
Denied
Edwards Lifescience, LLC has 1 FDA 510(k) cleared medical devices. Based in Irvine, US.
Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Edwards Lifescience, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Edwards Lifescience, LLC
1 devices