Ind Diagnostic, Inc. is one of 691 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Ind Diagnostic, Inc. - FDA 510(k) Cleared Devices
Recent clearances: IND URINARY TRACT INFECTION (UTI) TEST STRIPS, IND ONE STEP FECAL OCCULT BLOOD TEST MODEL 440-10, URINE CHEMISTRY ANALYZER UR-50
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.
510(k) submissions have been managed by Citech as regulatory consultant.
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