Smarttarget, Ltd. is one of 470 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Smarttarget, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: SmartTarget
1
Total
1
Cleared
0
Denied
Smarttarget, Ltd. has 1 FDA 510(k) cleared medical devices. Based in London, GB.
Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Smarttarget, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Smarttarget, Ltd.
1 devices