Aggredyne, Inc. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Aggredyne, Inc. has 3 FDA 510(k) cleared medical devices. Based in Houston, US.
Historical record: 3 cleared submissions from 2013 to 2019. Primary specialty: Hematology.
Browse the FDA 510(k) cleared devices submitted by Aggredyne, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Aggredyne, Inc.
3 devices