Ambicare Health, Ltd. is one of 437 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Ambicare Health, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Lustre PRO Light System
1
Total
1
Cleared
0
Denied
Ambicare Health, Ltd. has 1 FDA 510(k) cleared medical devices. Based in Livingston, GB.
Historical record: 1 cleared submissions from 2016 to 2016. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Ambicare Health, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Ismart Marketing Services, Ltd. as regulatory consultant.
FDA 510(k) Regulatory Record - Ambicare Health, Ltd.
1 devices