Genetic Testing Institute is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Genetic Testing Institute - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Genetic Testing Institute has 6 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 6 cleared submissions from 1984 to 2008. Primary specialty: Hematology.
Browse the FDA 510(k) cleared devices submitted by Genetic Testing Institute Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Genetic Testing Institute
6 devices
Cleared
Nov 20, 2008
FACTOR VIII ANTIBODY SCREEN
Hematology
107d
Cleared
Dec 19, 2007
PF4 IGG
Hematology
170d
Cleared
Jan 20, 2006
PF4 ENHANCED SOLID PHASE ELISA
Hematology
30d
Cleared
Feb 01, 2000
GTI-FVIII INHIBITOR ASSAY
Hematology
104d
Cleared
Mar 09, 1999
GTI-PF4 ELISA
Hematology
165d
Cleared
Jun 14, 1984
ALLO-TYPE HUMAN IMMUNOGLOBULIN-
Immunology
91d