Medical Device Manufacturer · US , Fort Worth , TX

Prestige Ameritech - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2006

Total

Cleared

Denied

Prestige Ameritech has 5 FDA 510(k) cleared medical devices. Based in Fort Worth, US.

Latest FDA clearance: Sep 2024. Active since 2006. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Prestige Ameritech Filter by specialty or product code using the sidebar.

Prestige Ameritech is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Prestige Ameritech

5 devices

1-5 of 5