Medivent Limited is one of 467 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Medivent Limited - FDA 510(k) Cleared Devices
Recent clearances: RTX RESPIRATOR
1
Total
1
Cleared
0
Denied
Medivent Limited has 1 FDA 510(k) cleared medical devices. Based in London, England, GB.
Historical record: 1 cleared submissions from 2008 to 2008. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Medivent Limited Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.
FDA 510(k) Regulatory Record - Medivent Limited
1 devices