Resoundant, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Resoundant, Inc. has 2 FDA 510(k) cleared medical devices. Based in Rochester, US.
Historical record: 2 cleared submissions from 2019 to 2020. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Resoundant, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Resoundant, Inc.
2 devices