FDA 510(k) Applications for Medical Device Product Code "KMI"
|
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 |