Medical Device Manufacturer · US , Walker , MI

Kabivitrum, Inc. - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 1981

8

Total

8

Cleared

0

Denied

Kabivitrum, Inc. has 8 FDA 510(k) cleared medical devices. Based in Walker, US.

Historical record: 8 cleared submissions from 1981 to 1988. Primary specialty: Hematology.

Browse the FDA 510(k) cleared devices submitted by Kabivitrum, Inc. Filter by specialty or product code using the sidebar.

8 devices

1–8 of 8

COATEST PROTEIN C

K884058 · GGP Test, Qualitative And Quantitative Factor Deficiency · Hematology

COATEST PLASMINOGEN

K854572 · DDX Plasminogen, Antigen, Antiserum, Control · Hematology

K844664 · KPE Container, I.v. · General Hospital

COATEST ANTIPLASMIN

K833890 · LGP Assay, Alpha-2-antiplasmin · Hematology

COATEST HEPARIN

K833891 · KFF Assay, Heparin · Hematology

COATEST FACTOR VIII

K833892 · GGP Test, Qualitative And Quantitative Factor Deficiency · Hematology

COATEST FACTOR X

K832114 · GGP Test, Qualitative And Quantitative Factor Deficiency · Hematology

COATEST ANTITHROMBIN

K812829 · JBQ Antithrombin Iii Quantitation · Hematology