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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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