Resoundant, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Resoundant, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Resoundant Acoustic Driver System, MREplus+ Software
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.
510(k) submissions have been managed by Hrg as regulatory consultant.
FDA 510(k) Regulatory Record - Resoundant, Inc.
2 devices