Eswallow USA is one of 5297 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: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Eswallow USA Filter by specialty or product code using the sidebar.
Eswallow USA — FDA 510(k) Products and Clearance History
2 devices
Cleared
Jan 25, 2013
ESWALLOW USA ELECTRODE,ESWALLOW USA LEADWIRE
Neurology
436d
Cleared
Feb 10, 2011
ESWALLOW DYSPHAGIA THERAPY KIT, PMI DYSPHAGIA THERAPY KIT
Physical Medicine
568d