Alexon Biomedical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Alexon Biomedical, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Alexon Biomedical, Inc. has 5 FDA 510(k) cleared medical devices. Based in Glen Ellyn, US.
Historical record: 5 cleared submissions from 1988 to 1997. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Alexon Biomedical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Alexon Biomedical, Inc.
5 devices
Cleared
Feb 04, 1997
PROSPECT II CLOSTRIDIUM DIFFILLIE TOXIN A MICROPLATE ASSAY
Microbiology
62d
Cleared
Feb 09, 1996
PROSPECT GIARDIA/CRYPTOSPORIDIUM MICROPLATE ASSAY
Microbiology
88d
Cleared
Nov 17, 1994
PROSPECT CRYPTOSPORIDIUM RAPID ASSAY
Microbiology
329d
Cleared
Nov 22, 1993
PROSPECT ENTAMOEBA HISTOLYTICA MICROPLATE ASSAY
Microbiology
97d
Cleared
Jan 05, 1988
PROSPECT/GIARDIA
Microbiology
41d