# Biovation, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 11 (1978–1993): 11 510(k) clearances
- Product codes: JQP (4), GKZ (2), JQX (2), JGP (1), JRE (1), JJQ (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K925528: Biovation K-Manager (Feb 5, 1993)
- K923844: Lyris 100/120 Laboratory Information System (Dec 11, 1992)
- K915071: Differential Counting Board (Jan 17, 1992)
- K853026: Biovation Max Data Management System (Aug 2, 1985)
- K842401: Chemistry Console (Sep 4, 1984)
- K831830: Lyris Modular Info System (Jun 25, 1984)
- K821534: Hematology Data Management Sys (Jun 10, 1982)
- K812604: Biovation Urinalysis Reporter (Oct 2, 1981)

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