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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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