FDA 510(k) Applications for Medical Device Product Code "KMI"
(Monitor, Bed Patient)

FDA 510(k) Number Applicant Device Name Decision Date
K090138 AFRAME DIGITAL, INC. MOBILECARE MONITOR, MODEL 2100 04/24/2009
K130752 CENTAURI MEDICAL, INC. DYNASENSE SYSTEM 08/15/2013
K131585 INTEL-GE CARE INNOVATIONS LLC INTEL-GE CARE INNOVATIONS QUIETCARE 10/08/2013
K141877 LEAF HEALTHCARE, INC. LEAF PATIENT MONITORING SYSTEM 11/10/2014
K101109 WIRELESS MEDCARE, LLC VIVATRAK 07/15/2010


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