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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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