Medical Device Manufacturer · US , Braintree , MA

Cruzar Medsystems, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2015

Total

Cleared

Denied

Cruzar Medsystems, Inc. has 2 FDA 510(k) cleared medical devices. Based in Braintree, US.

Last cleared in 2022. Active since 2015. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Cruzar Medsystems, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Cruzar Medsystems, Inc.

2 devices

1-2 of 2