Medical Device Manufacturer · ID , Bandung

N.V. Kalibaru - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1989

Total

Cleared

Denied

N.V. Kalibaru has 1 FDA 510(k) cleared medical devices. Based in Bandung, ID.

Historical record: 1 cleared submissions from 1989 to 1989. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by N.V. Kalibaru Filter by specialty or product code using the sidebar.

N.V. Kalibaru is one of 6 FDA 510(k) medical device manufacturers from Indonesia in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - N.V. Kalibaru

1 devices

1-1 of 1