Bayer Corp. - FDA 510(k) Cleared Devices
96
Total
96
Cleared
0
Denied
FDA 510(k) Regulatory Record - Bayer Corp. Microbiology ✕
6 devices
Cleared
Aug 20, 2001
BAYER DIAGNOSTICS ADVIA CENTAUR TOXOPLASMA IGM ASSAY
Microbiology
160d
Cleared
Jul 05, 2001
BAYER DIAGNOSTICS ADVIA CENTAUR RUBELLA IGM ASSAY
Microbiology
121d
Cleared
Apr 13, 2001
ADVIA CENTAUR RUBELLA IGG ASSAY
Microbiology
162d
Cleared
Oct 22, 1997
TOXOPLASMA IGM ASSAY FOR THE BAYER IMMUNO1 SYSTEM (IN VITRO DIAGNOSTIC SYSTEM)
Microbiology
146d
Cleared
Aug 02, 1996
TOXOPLASMA IGG IN-VITRO DIAGNOSTIC SYSTEM
Microbiology
226d
Cleared
Apr 15, 1996
RUBELLA IGG ASSAY FOR THE TECHNICON IMMUNO 1 SYSTEM IN-VITRO DIAGNOSTIC DEVICE
Microbiology
385d