Dyansys Corp is one of 23717 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dyansys Corp - FDA 510(k) Cleared Devices
Recent clearances: PORTABLE ECSCOPE
1
Total
1
Cleared
0
Denied
Dyansys Corp has 1 FDA 510(k) cleared medical devices. Based in Burlingame, US.
Historical record: 1 cleared submissions from 2007 to 2007. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Dyansys Corp Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Dyansys Corp
1 devices