Icare Newlife Technologies, Inc. is one of 2177 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.
Icare Newlife Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Fetal Doppler
1
Total
1
Cleared
0
Denied
Icare Newlife Technologies, Inc. has 1 FDA 510(k) cleared medical devices. Based in Beijing, CN.
Historical record: 1 cleared submissions from 2015 to 2015. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Icare Newlife Technologies, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Guangzhou Osmunda Medical Device Consulting Co., Ltd. as regulatory consultant.
FDA 510(k) Regulatory Record - Icare Newlife Technologies, Inc.
1 devices