Datascope Corp. - FDA 510(k) Cleared Devices

Datascope Corp. has 135 FDA 510(k) cleared cardiovascular devices. Based in Mchenry, US.

Historical record: 135 cleared submissions from 1976 to 2019.

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 Underwriters Laboratories, Inc. as regulatory consultant.