Prestige Ameritech , Ltd. is one of 4785 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Prestige Ameritech , Ltd. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Prestige Ameritech , Ltd. has 1 FDA 510(k) cleared medical devices. Based in North Richland Hills, US.
Historical record: 1 cleared submissions from 2016 to 2016. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Prestige Ameritech , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Prestige Ameritech , Ltd.
1 devices