Creavo Medical Technologies, Ltd. is one of 462 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Creavo Medical Technologies, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Creavo Vitalscan Magnetocardiograph
1
Total
1
Cleared
0
Denied
Creavo Medical Technologies, Ltd. has 1 FDA 510(k) cleared medical devices. Based in Coventry, GB.
Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Creavo Medical Technologies, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Halloran Consulting Group, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Creavo Medical Technologies, Ltd.
1 devices