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.


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact