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FDA 510(k) Applications Submitted by OSTAR MEDITECH CORP.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K050680
03/16/2005
BLOOD PRESSURE MONITOR WITH SPECTRUM/P2, X2, A2, AND K7
OSTAR MEDITECH CORP.
K112269
08/08/2011
OSTAR USB BLOOD PRESSURE MONITOR WITH SPECTRUM / P200 FOR UPPER ARM, AND M100 FOR WRIST TYPE
OSTAR MEDITECH CORP.
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