Ddat(Uk), Ltd. is one of 520 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
1
Total
1
Cleared
0
Denied
Ddat(Uk), Ltd. has 1 FDA 510(k) cleared medical devices. Based in Basingstoke, Hampshire, GB.
Historical record: 1 cleared submissions from 2005 to 2005. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Ddat(Uk), 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 - Ddat(Uk), Ltd.
1 devices