Medical Device Manufacturer · US , Walker , MI

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

8 submissions · 8 cleared · Since 1981

Total

Cleared

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.

Kabivitrum, Inc. 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 - Kabivitrum, Inc.

8 devices

1-8 of 8