Ind Diagnostic, Inc. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Ind Diagnostic, Inc. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Ind Diagnostic, Inc. has 8 FDA 510(k) cleared medical devices. Based in Delta, B.C., CA.
Historical record: 8 cleared submissions from 2003 to 2012. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Ind Diagnostic, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ind Diagnostic, Inc.
8 devices
Cleared
Apr 17, 2012
IND URINARY TRACT INFECTION (UTI) TEST STRIPS
Chemistry
551d
Cleared
Jul 19, 2010
IND ONE STEP FECAL OCCULT BLOOD TEST MODEL 440-10
Hematology
194d
Cleared
Mar 01, 2007
URINE CHEMISTRY ANALYZER UR-50
Chemistry
112d
Cleared
Aug 07, 2006
ONE STEP DRUG TEST - AMP/MET/MOR/THC/COC
Toxicology
136d
Cleared
Dec 16, 2005
ONE STEP HCG PREGNANCY TEST - 2000 MIU/ML, MODEL 100 SERIES.
Chemistry
79d
Cleared
Nov 30, 2005
ONE STEP FSH MENOPAUSAL TEST
Chemistry
64d
Cleared
May 16, 2005
IND ONE STEP HCG PREGNANCY TEST - CASSETTE FORMAT
Chemistry
56d
Cleared
Jan 03, 2003
CASSETTE/URINE HCG
Chemistry
65d