Medical Device Manufacturer · CA , Waterloo, On

Mespere Lifesciences, Inc. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2013

Total

Cleared

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.

Mespere Lifesciences, Inc. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Mespere Lifesciences, Inc.

3 devices

1-3 of 3