Picopack, Inc. - FDA 510(k) Cleared Devices

Picopack, Inc. has 1 FDA 510(k) cleared medical devices. Based in Daejeon, KR.

Last cleared in 2023. Active since 2023. Primary specialty: Radiology.

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

510(k) submissions have been managed by Lighten Bridge, LLC as regulatory consultant.