# Kabivitrum, Inc.

- Location (FDA's records): Walker, MI
- FDA decisions: 8 (1981–1988): 8 510(k) clearances
- Product codes: GGP (3), JBQ (1), KPE (1), LGP (1), KFF (1), DDX (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 5 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Instrumentation Laboratory CO: 5 (https://510kreport.com/company/instrumentation-laboratory)

## Its most-cited devices
- K833892: Coatest Factor Viii (1984), cited by 3
- K833890: Coatest Antiplasmin (1984), cited by 1
- K854572: Coatest Plasminogen (1986), cited by 1

## Recent decisions
- K884058: Coatest Protein C (Dec 13, 1988)
- K854572: Coatest Plasminogen (Feb 26, 1986)
- K844664: The I.V. Bag (May 6, 1985)
- K833892: Coatest Factor Viii (Jan 30, 1984)
- K833890: Coatest Antiplasmin (Jan 30, 1984)
- K833891: Coatest Heparin (Jan 30, 1984)
- K832114: Coatest Factor X (Aug 26, 1983)
- K812829: Coatest Antithrombin (Dec 30, 1981)

Source page: https://510kreport.com/company/kabivitrum