FDA 510(k) Applications Submitted by MEDITECH KFT.

FDA 510(k) Number Submission Date Device Name Applicant
K051149 05/04/2005 MEDITECH MODEL ABPM-04 MEDITECH KFT.
K071960 07/16/2007 MEDITECH AMBULATORY BLOOD PRESSURE MONITOR, MODEL ABPM-05 MEDITECH KFT.


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