Bd Kiestra B.V. is one of 68 FDA 510(k) medical device manufacturers from Netherlands in the dataset, ranked by real submission volume.
Bd Kiestra B.V. - FDA 510(k) Cleared Devices
Recent clearances: BD Kiestra Methicillin-resistant Staphylococcus aureus (MRSA) Application, BD Kiestra MRSA App
1
Total
1
Cleared
0
Denied
Bd Kiestra B.V. has 1 FDA 510(k) cleared medical devices. Based in Drachten, NL.
Last cleared in 2023. Active since 2023. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Bd Kiestra B.V. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Bd Kiestra B.V.
1 devices