FDA 510(k) Applications Submitted by JESSICA TUNG

FDA 510(k) Number Submission Date Device Name Applicant
K120064 01/09/2012 TEST, BLOOD GLUCOSE SYSTEM HMD BIOMEDICAL, INC.
K121433 05/14/2012 GOODLIFE CS-200 (SINGLE PATIENT USE), CS-200 PROFESSIONAL (MULTIPLE PATIENT USE) BLOOD GLUCOSE MONITORING SYSTEMS HMD BIOMEDICAL, INC.
K113307 11/08/2011 GL GOODLIFE SERIES BLOOD GLUCOSE MONITORING SYSMTEM HMD BIOMEDICAL, INC.


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