Voxar Limited is one of 507 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Voxar Limited - FDA 510(k) Cleared Devices
Recent clearances: VOXAR 3D PRODUCT FAMILY, VOXAR'S CALCIUM SCORING PRODUCT, VOXAR VC, MODEL 1.0
4
Total
4
Cleared
0
Denied
Voxar Limited has 4 FDA 510(k) cleared medical devices. Based in Edinburgh, Lothian, GB.
Historical record: 4 cleared submissions from 1999 to 2005. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Voxar Limited Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Voxar Limited
4 devices