Mediwatch Plc is one of 520 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Mediwatch Plc - FDA 510(k) Cleared Devices
Recent clearances: PORTASCAN BLADDER SCANNER, MODEL PA00146
1
Total
1
Cleared
0
Denied
Mediwatch Plc has 1 FDA 510(k) cleared medical devices. Based in Rugby, Warwickshire, GB.
Historical record: 1 cleared submissions from 2003 to 2003. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Mediwatch Plc 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 Plc
1 devices