Mesa Laboratories, Inc. - FDA 510(k) Cleared Devices

Mesa Laboratories, Inc. has 9 FDA 510(k) cleared medical devices. Based in Lakewood, US.

Historical record: 9 cleared submissions from 2004 to 2020. Primary specialty: Gastroenterology & Urology.

Browse the FDA 510(k) cleared devices submitted by Mesa Laboratories, Inc. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Ibp Medical GmbH as regulatory consultant.