FDA 510(k) Applications Submitted by SENSACARE LTD.

FDA 510(k) Number Submission Date Device Name Applicant
K070086 01/09/2007 SENSACARE MODEL SAA-102 ARM TYPE DIGITAL BLOOD PRESSURE MONITOR SENSACARE LTD.
K061935 07/10/2006 SENSACARE SAW-102 WRIST DIGITAL BLOOD PRESSURE MONITOR SENSACARE LTD.


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