Positrigo AG - FDA 510(k) Cleared Devices

Positrigo AG has 1 FDA 510(k) cleared medical devices. Based in Z?rich, CH.

Latest FDA clearance: Jul 2024. Active since 2024. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Positrigo AG Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Third Party Review Group, LLC as regulatory consultant.