Kabi Pharmacia, Inc. is one of 26109 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kabi Pharmacia, Inc. - FDA 510(k) Cleared Devices
Recent clearances: PHARMACIA CAP SYSTEM IGE FEIA -- MODIFICATION, COAMATE(R) ANTITHROMBIN CHROMOGENIC ASSAY
2
Total
2
Cleared
0
Denied
Kabi Pharmacia, Inc. has 2 FDA 510(k) cleared medical devices. Based in Franklin, US.
Historical record: 2 cleared submissions from 1992 to 1992. Primary specialty: Immunology.
Browse the FDA 510(k) cleared devices submitted by Kabi Pharmacia, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Kabi Pharmacia, Inc.
2 devices