Techmedic Development International B.V. is one of 143 FDA 510(k) medical device manufacturers from Netherlands in the dataset, ranked by real submission volume.
Techmedic Development International B.V. - FDA 510(k) Cleared Devices
Recent clearances: Dyna-Vision Telemonitoring System
1
Total
1
Cleared
0
Denied
Techmedic Development International B.V. has 1 FDA 510(k) cleared medical devices. Based in Broek Op Langedijk, NL.
Historical record: 1 cleared submissions from 2016 to 2016. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Techmedic Development International B.V. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Qserve Group, Us, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Techmedic Development International B.V.
1 devices