Deepsight NeedleVue LC1 Ultrasound System
Aug 2025
171d
DeepSight Technology, Inc.
1
Total
1
Cleared
0
Denied
DeepSight Technology, Inc. — FDA 510(k) Submissions
DeepSight Technology, Inc. has submitted 1 FDA 510(k) premarket notifications since 2025, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include System, Imaging, Pulsed Echo, Ultrasonic . Use the specialty filter in the sidebar to narrow results.
1 devices