Mediwatch, Ltd. is one of 508 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Mediwatch, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: MEDIWATCH MULTISCAN ULTRASOUND SYSTEM/SCANNER, MODEL M0002 (SCANNER ONLY)
1
Total
1
Cleared
0
Denied
Mediwatch, Ltd. has 1 FDA 510(k) cleared medical devices. Based in Warwickshire, GB.
Historical record: 1 cleared submissions from 2005 to 2005. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Mediwatch, Ltd. 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 - Mediwatch, Ltd.
1 devices