Biovation, Inc.
Biovation, Inc. holds FDA 510(k) medical device clearances, first cleared 1978, most recent 1993.
Top product codes for Biovation, Inc.
Recent clearances by Biovation, Inc.
- K925528 — BIOVATION K-MANAGER
- K923844 — LYRIS 100/120 LABORATORY INFORMATION SYSTEM
- K915071 — DIFFERENTIAL COUNTING BOARD
- K853026 — BIOVATION MAX DATA MANAGEMENT SYSTEM
- K842401 — CHEMISTRY CONSOLE
- K831830 — LYRIS MODULAR INFO SYSTEM
- K821534 — HEMATOLOGY DATA MANAGEMENT SYS
- K812604 — BIOVATION URINALYSIS REPORTER
- K792045 — BIOVATION NEPHELOMETER
- K790862 — BIOVATION DIGITAL URINOMETER
- K781644 — ANTIBIOTIC NEPHELOMETER
Data sourced from openFDA. This site is unofficial and independent of the FDA.