Cruzar Medsystems, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cruzar Medsystems, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Houdini Cross Support Catheter
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.
FDA 510(k) Regulatory Record - Cruzar Medsystems, Inc.
2 devices