Meridian Technique, Ltd. is one of 467 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Meridian Technique, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: OrthoView 7.2
1
Total
1
Cleared
0
Denied
Meridian Technique, Ltd. has 1 FDA 510(k) cleared medical devices. Based in Southhampton, GB.
Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Meridian Technique, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Third Party Review Group, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Meridian Technique, Ltd.
1 devices