Post Oak Innovations, Inc. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Post Oak Innovations, Inc. has 1 FDA 510(k) cleared medical devices. Based in Austin, US.
Historical record: 1 cleared submissions from 2012 to 2012. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Post Oak Innovations, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Post Oak Innovations, Inc.
1 devices