Mespere Lifesciences, Inc. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Mespere Lifesciences, Inc. has 3 FDA 510(k) cleared medical devices. Based in Waterloo, On, CA.
Historical record: 3 cleared submissions from 2013 to 2018. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Mespere Lifesciences, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Mespere Lifesciences, Inc.
3 devices