Lake Region Mfg., Inc. - FDA 510(k) Cleared Devices

Lake Region Mfg., Inc. has 42 FDA 510(k) cleared cardiovascular devices. Based in Mchenry, US.

Historical record: 42 cleared submissions from 1977 to 2010.

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 Regulatory Technology Services, LLC as regulatory consultant.