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FDA 510(k) Applications Submitted by KAI LOU
FDA 510(k) Number
Submission Date
Device Name
Applicant
K110889
03/30/2011
IND ONE STEP HCG URINE PREGNANCY TEST (STRIP)
IND DIAGNOSTICS INC.
K121231
04/24/2012
IND DRUG HOME MULTI-PANEL TEST (2-5) IND MORPHINE HOME TEST
IND NDIAGNOSTIC INC.
K103037
10/14/2010
IND URINARY TRACT INFECTION (UTI) TEST STRIPS
IND DIAGNOSTIC, INC.
K113506
11/28/2011
IND ONE STEP OCCULT BLOOD (FOB) TEST
IND DIAGNOSTICS INC.
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