Neural Analytics, Inc. is one of 13640 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Neural Analytics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: NeuralBot, Lucid M1 Transcranial Doppler Ultrasound System (Lucid M1 System) with 2MHz Transducers
2
Total
2
Cleared
0
Denied
Neural Analytics, Inc. has 2 FDA 510(k) cleared medical devices. Based in Los Angeles, US.
Historical record: 2 cleared submissions from 2016 to 2018. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Neural Analytics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Neural Analytics, Inc.
2 devices