Neurophet., Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Neurophet., Inc. has 4 FDA 510(k) cleared medical devices. Based in Seoul, KR.
Latest FDA clearance: Jan 2026. Active since 2022. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Neurophet., Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by LK Consulting Group USA, Inc. and Global Medical Standard Consulting Co., Ltd..
4 devices