Cellreturn Co., Ltd. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Cellreturn Co., Ltd. has 1 FDA 510(k) cleared medical devices. Based in Incheon, KR.
Last cleared in 2022. Active since 2022. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Cellreturn Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Bt Solutions, Inc. as regulatory consultant.
1 devices