Medical Device Manufacturer · US , Danville , CA

Kabi Diagnostica - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1990

Total

Cleared

Denied

Kabi Diagnostica has 2 FDA 510(k) cleared medical devices. Based in Danville, US.

Historical record: 2 cleared submissions from 1990 to 1990. Primary specialty: Hematology.

Browse the FDA 510(k) cleared devices submitted by Kabi Diagnostica Filter by specialty or product code using the sidebar.

Kabi Diagnostica is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Kabi Diagnostica

2 devices

1-2 of 2

Data Source

Sourced from the FDA 510(k) public files . 175,218 total devices indexed.

Last updated: Apr 28, 2026