Cardiovascular Systems, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cardiovascular Systems, Inc. - FDA 510(k) Cleared Devices
Recent clearances: DIAMONDBACK 360 Peripheral Orbital Atherectomy System, DIAMONDBACK 360 Peripheral Orbital Atherectomy System, Exchangeable Series, Stealth 360 Peripheral Orbital Atherectomy System, ViperCross Support Catheters, Diamonback 360 Peripheral Orbital Atherectomy System, Diamondback 360 Stealth Orbital Atherectomy system
Cardiovascular Systems, Inc. has 26 FDA 510(k) cleared cardiovascular devices. Based in Saint Paul, US.
Last cleared in 2022. Active since 2007.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Biomerics as regulatory consultant.