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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