Eswallow USA is one of 5700 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Eswallow USA - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Eswallow USA has 2 FDA 510(k) cleared medical devices. Based in Naples, US.
Historical record: 2 cleared submissions from 2011 to 2013. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Eswallow USA Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Eswallow USA
2 devices