Theratest Laboratories, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Theratest Laboratories, Inc. - FDA 510(k) Cleared Devices
22
Total
22
Cleared
0
Denied
Theratest Laboratories, Inc. has 22 FDA 510(k) cleared immunology devices. Based in Chicago, US.
Historical record: 22 cleared submissions from 1991 to 2010.
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 - Theratest Laboratories, Inc.
22 devices
Cleared
Mar 05, 2010
THERATEST EL-ANTI-CCP/2
Immunology
350d
Cleared
Sep 03, 2009
THERATEST EL-ANTI-TPO AND THERATEST EL-ANTI-THYROGLOBULIN, MODEL 104-119,...
Immunology
164d
Cleared
Nov 05, 2007
THERATEST EL-TTG IGA/IGG AND THERATEST EL-GLIA IGA/IGG TEST SYSTEMS
Immunology
138d
Cleared
Jul 20, 2006
EL-ANCA: ANTI-MPO, ANTI-PR3, ANTI-MPO AND ANTI-PR3
Immunology
64d
Cleared
Feb 07, 2006
EL-ACL SCREEN
Immunology
15d
Cleared
Oct 07, 2005
THERATEST EL-ANA PROFILES
Immunology
164d
Cleared
Mar 11, 2004
EL-ANA PROFILES: ANTI-CHROMATIN
Immunology
34d
Cleared
Feb 06, 2003
THE THERATEST EL-ANA PROFILES: ANTI-CENTROMERE
Immunology
62d
Cleared
Feb 06, 2003
EL-ANA PROFILES: ANTI-RIBOSOMAL PROTEIN P
Immunology
62d
Cleared
Sep 12, 2000
EL-ANA PROFILES-2K1
Immunology
26d
Cleared
Aug 13, 1998
EL-ANA PROFILES: EL-ENA/4
Immunology
56d
Cleared
Aug 13, 1998
EL-ANA PROFILES: EL-ENA/5
Immunology
56d