Biovation, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Biovation, Inc. - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
Biovation, Inc. has 11 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 11 cleared submissions from 1978 to 1993. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Biovation, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Biovation, Inc.
11 devices
Cleared
Feb 05, 1993
BIOVATION K-MANAGER
Hematology
95d
Cleared
Dec 11, 1992
LYRIS 100/120 LABORATORY INFORMATION SYSTEM
Chemistry
133d
Cleared
Jan 17, 1992
DIFFERENTIAL COUNTING BOARD
Hematology
70d
Cleared
Aug 02, 1985
BIOVATION MAX DATA MANAGEMENT SYSTEM
Chemistry
15d
Cleared
Sep 04, 1984
CHEMISTRY CONSOLE
Chemistry
77d
Cleared
Jun 25, 1984
LYRIS MODULAR INFO SYSTEM
Chemistry
384d
Cleared
Jun 10, 1982
HEMATOLOGY DATA MANAGEMENT SYS
Hematology
17d
Cleared
Oct 02, 1981
BIOVATION URINALYSIS REPORTER
Chemistry
17d
Cleared
Oct 30, 1979
BIOVATION NEPHELOMETER
Chemistry
18d
Cleared
Jun 28, 1979
BIOVATION DIGITAL URINOMETER
Chemistry
52d
Cleared
Oct 03, 1978
ANTIBIOTIC NEPHELOMETER
Microbiology
8d