Corgenix, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Corgenix, Inc. - FDA 510(k) Cleared Devices
23
Total
23
Cleared
0
Denied
Corgenix, Inc. has 23 FDA 510(k) cleared immunology devices. Based in Westminster, US.
Historical record: 23 cleared submissions from 1998 to 2008.
Browse the complete list of FDA 510(k) cleared immunology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Corgenix, Inc.
23 devices
Cleared
Apr 04, 2008
IGG ANTI-ATHEROX TEST KIT
Immunology
255d
Cleared
May 29, 2007
ASPIRINWORKS TEST KIT (11-DEHYDRO THROMBOXANE B2), MODEL 12136
Hematology
315d
Cleared
Nov 19, 2004
RHIGENE HEP-ANA TEST SYSTEM
Immunology
51d
Cleared
Apr 05, 2004
REAADS VON WILLEBRAND FACTOR ACTIVITY TEST KIT, MODEL 10826
Hematology
269d
Cleared
Jan 08, 2004
REAADS DSDNA QUANTITATIVE TEST KIT, MODEL 022-001
Immunology
15d
Cleared
Oct 14, 2003
REAADS II ANTI-CARDIOLIPIN IGG SEMI-QUANTITATIVE TEST KIT, MODEL 11139
Immunology
29d
Cleared
Jul 07, 2003
REAADS IGM ANTI-B2GPI TEST KIT, MODEL 038-001
Immunology
81d
Cleared
Jan 03, 2003
MODIFICATION TO REAADS ANTI-PHOSPHATIDYLSERINE IGA SEMI-QUANTATIVE TEST KIT
Immunology
14d
Cleared
Jan 03, 2003
REEADS ANTI-PHOSPHATIDYLSERINE IGG/IGM SEMI-QUANTITATIVE TEST KIT
Immunology
14d
Cleared
Sep 25, 2002
REAADS IGA ANTI-CARDIOLIPIN SEMI-QUANTITATIVE TEST KIT, MODEL 026-001
Immunology
16d
Cleared
Sep 25, 2002
REAADS ANTI-CARDIOLIPIN IGG/IGM SEMI-QUANTITATIVE TEST KIT, MODEL 023-001
Immunology
16d
Cleared
Sep 28, 2001
REAADS ANTI-BETA 2 GLYCOPROTEIN I IGM TEST KIT
Immunology
14d