Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Biovation, Inc.

FDA 510(k) & PMA Approved Devices — 11 products

Total Devices11

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K925528	BIOVATION K-MANAGER	GKZ	1993-02-05	View
510(k)	K923844	LYRIS 100/120 LABORATORY INFORMATION SYSTEM	JJQ	1992-12-11	View
510(k)	K915071	DIFFERENTIAL COUNTING BOARD	GKZ	1992-01-17	View
510(k)	K853026	BIOVATION MAX DATA MANAGEMENT SYSTEM	JQP	1985-08-02	View
510(k)	K842401	CHEMISTRY CONSOLE	JQP	1984-09-04	View
510(k)	K831830	LYRIS MODULAR INFO SYSTEM	JQP	1984-06-25	View
510(k)	K821534	HEMATOLOGY DATA MANAGEMENT SYS	JGP	1982-06-10	View
510(k)	K812604	BIOVATION URINALYSIS REPORTER	JQP	1981-10-02	View
510(k)	K792045	BIOVATION NEPHELOMETER	JQX	1979-10-30	View
510(k)	K790862	BIOVATION DIGITAL URINOMETER	JRE	1979-06-28	View
510(k)	K781644	ANTIBIOTIC NEPHELOMETER	JQX	1978-10-03	View

↑