Armbrust, Inc. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Armbrust, Inc. has 1 FDA 510(k) cleared medical devices. Based in Pflugerville, US.
Last cleared in 2022. Active since 2022. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Armbrust, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Armbrust, Inc.
1 devices