Meditera Tibbi Malzeme San VE Tic AS is one of 37 FDA 510(k) medical device manufacturers from Turkey in the dataset, ranked by real submission volume.
Meditera Tibbi Malzeme San VE Tic AS - FDA 510(k) Cleared Devices
Recent clearances: Altech® Exhalation Valve (Single Limb and Dual Limb), Altera Filter and HME/Filter, Altera gas Sampling Lines
3
Total
3
Cleared
0
Denied
Meditera Tibbi Malzeme San VE Tic AS has 3 FDA 510(k) cleared medical devices. Based in Izmir, TR.
Last cleared in 2021. Active since 2020. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Meditera Tibbi Malzeme San VE Tic AS Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Meditera Tibbi Malzeme San. VE Tic. A.S. % Promedic, LLC and Meditera Tibbi Malzeme San VE Tic AS C/O Promedic, LLC.
FDA 510(k) Regulatory Record - Meditera Tibbi Malzeme San VE Tic AS
3 devices