Medical Device Manufacturer · NL , Drachten

Bd Kiestra B.V. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2023
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) cleared devices by Bd Kiestra B.V.

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