Am USA is one of 5120 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Am USA - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Am USA has 4 FDA 510(k) cleared medical devices. Based in Nashville, US.
Historical record: 4 cleared submissions from 2011 to 2014. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Am USA Filter by specialty or product code using the sidebar.
Am USA — FDA 510(k) Products and Clearance History
4 devices
Cleared
Aug 13, 2014
0.9% SODIUM CHLORIDE FLUSH SYRINGE
General Hospital
254d
Cleared
Jul 12, 2012
0.9% SODIUM CHLORIDE FLISH SYRINGE
General Hospital
114d
Cleared
Jan 30, 2012
AM USA 0.9% SODIUM CHLORIDE FLUSH SYRINGE
General Hospital
60d
Cleared
Jul 14, 2011
AM USA 0.9% SODIUM CHLORIDE FLUSH SYRINGE
General Hospital
92d