Immuno-Mycologics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Immuno-Mycologics, Inc. - FDA 510(k) Cleared Devices
26
Total
26
Cleared
0
Denied
Immuno-Mycologics, Inc. has 26 FDA 510(k) cleared microbiology devices. Based in Mchenry, US.
Historical record: 26 cleared submissions from 1979 to 2012.
Browse the complete list of FDA 510(k) cleared microbiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Immuno-Mycologics, Inc.
26 devices
Cleared
Dec 17, 2012
ALPHA CRYPTOCOCCAL ANTIGEN EIA
Microbiology
263d
Cleared
Mar 28, 2012
CRAG LATERAL FLOW ASSAY (LFA)
Microbiology
218d
Cleared
Jul 20, 2011
CRAG LATERAL FLOW ASSAY (CRAG LFA)
Microbiology
342d
Cleared
Jul 19, 2011
ALPHA HISTOPLASMA ANTIGEN EIA MODEL HAG102
Microbiology
426d
Cleared
Aug 25, 1988
RABBIT PLASMA FIBRINOGEN (RPF) SUPPLEMENT
Microbiology
16d
Cleared
Feb 24, 1988
EXO-ANTIGEN IDENTIFICATION SYSTEM CAT.# EX1001
Microbiology
50d
Cleared
Oct 01, 1984
EI-CANDIDA ENZYME IMMUNOASSAY EI1001
Microbiology
41d
Cleared
Jun 08, 1983
LA-STAPH IDENTIFICATION SYSTEM
Microbiology
Cleared
May 05, 1983
LA-HISTO ANTIBODY SYSTEM #HL 1001
Microbiology
50d
Cleared
Mar 20, 1981
YA-CRYPTO ANTIBODY TUBE AGGLUTINATION
Microbiology
24d
Cleared
Oct 31, 1980
LA-SPORO ANTIBODY SYSTEM
Microbiology
25d
Cleared
Jun 02, 1980
CAPIK-CANDIDA ALBICANS IDENT. KIT.
Microbiology
42d