Ardent Sound, Inc. is one of 24545 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ardent Sound, Inc. - FDA 510(k) Cleared Devices
Recent clearances: VOYAGER COMPACT IMAGING SYSTEM, SEEKER/SPARK ULTRASOUND SYSTEM, VOYAGER PERSONAL IMAGING DEVICE
3
Total
3
Cleared
0
Denied
Ardent Sound, Inc. has 3 FDA 510(k) cleared medical devices. Based in Mesa, US.
Historical record: 3 cleared submissions from 2005 to 2009. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Ardent Sound, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Ardent Sound, Inc.
3 devices