Elaitra, Ltd. is one of 195 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Elaitra, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: ViewFinder Software Version 1.1
1
Total
1
Cleared
0
Denied
Elaitra, Ltd. has 1 FDA 510(k) cleared medical devices. Based in London, GB.
Last cleared in 2023. Active since 2023. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Elaitra, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Elaitra, Ltd.
1 devices