Sensydia, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sensydia, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Integrated CardioRespiratory System
1
Total
1
Cleared
0
Denied
Sensydia, Inc. has 1 FDA 510(k) cleared medical devices. Based in Los Angeles, US.
Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Sensydia, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Experien Group, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Sensydia, Inc.
1 devices