Hutom, Inc. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Hutom, Inc. has 1 FDA 510(k) cleared medical devices. Based in Seoul, KR.
Latest FDA clearance: Jul 2024. Active since 2024. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Hutom, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by LK Consulting Group USA, Inc. as regulatory consultant.
1 devices