FDA 510(k) Applications Submitted by IND DIAGNOSTIC INC.

FDA 510(k) Number Submission Date Device Name Applicant
K063390 11/09/2006 URINE CHEMISTRY ANALYZER UR-50 IND DIAGNOSTIC INC.
K023638 10/30/2002 CASSETTE/URINE HCG IND DIAGNOSTIC INC.
K100031 01/06/2010 IND ONE STEP FECAL OCCULT BLOOD TEST MODEL 440-10 IND DIAGNOSTIC INC.
K050741 03/21/2005 IND ONE STEP HCG PREGNANCY TEST - CASSETTE FORMAT IND DIAGNOSTIC INC.
K060810 03/24/2006 ONE STEP DRUG TEST - AMP/MET/MOR/THC/COC IND DIAGNOSTIC INC.
K052662 09/27/2005 ONE STEP FSH MENOPAUSAL TEST IND DIAGNOSTIC INC.
K052694 09/28/2005 ONE STEP HCG PREGNANCY TEST - 2000 MIU/ML, MODEL 100 SERIES. IND DIAGNOSTIC INC.


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