Chemicon Intl., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Chemicon Intl., Inc. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Chemicon Intl., Inc. has 8 FDA 510(k) cleared medical devices. Based in Temecula, US.
Historical record: 8 cleared submissions from 1995 to 1999. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Chemicon Intl., Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Chemicon Intl., Inc.
8 devices
Cleared
Aug 10, 1999
LIGHT DIAGNOSTICS PNEUMOCYSTIS CARINII DFA, MODEL 31965
Microbiology
35d
Cleared
Sep 12, 1995
ENTEROVIRUS BLEND MONOCLONAL ANTIBODIES
Microbiology
617d
Cleared
Sep 12, 1995
ENTEROVIRUS 71 MONOCLONAL ANTIBODY
Microbiology
587d
Cleared
Sep 08, 1995
ENTEROVIRUS MONOCL ANTIBODY DET OF COXSACKIE A9 VIRUS
Microbiology
627d
Cleared
Sep 08, 1995
COXSACKIE A24 VIRUS MONOCLONAL ANTIBODY
Microbiology
626d
Cleared
Sep 08, 1995
COXSACKIEVIRUS B1 MONOCLONAL ANTIBODY
Microbiology
620d
Cleared
Sep 08, 1995
COXSACKIEVIRUS B BLEND MONOCLONAL ANTIBODIES
Microbiology
583d
Cleared
Sep 08, 1995
COXSACKIEVIRUS B5 MONOCLONAL ANTIBODY
Microbiology
583d