Medical Device Manufacturer · US , Centennial , CO

Allosource, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2008

Total

Cleared

Denied

Allosource, Inc. has 2 FDA 510(k) cleared medical devices. Based in Centennial, US.

Historical record: 2 cleared submissions from 2008 to 2011. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Allosource, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Allosource, Inc.

2 devices

1-2 of 2