Cruzar Medsystems, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
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.
510(k) submissions have been managed by Strategic Quality Solutions, LLC as regulatory consultant.
2 devices